Item | Value |
---|---|
geneid | 3973 |
ensemblid | ENSG00000138039.15 |
hgncid | 6585 |
symbol | LHCGR |
name | luteinizing hormone/choriogonadotropin receptor |
refseq_nuc | NM_000233.4 |
refseq_prot | NP_000224.2 |
ensembl_nuc | ENST00000294954.12 |
ensembl_prot | ENSP00000294954.6 |
mane_status | MANE Select |
chr | chr2 |
start | 48686774 |
end | 48755724 |
strand | - |
ver | v1.2 |
region | chr2:48686774-48755724 |
region5000 | chr2:48681774-48760724 |
regionname0 | LHCGR_chr2_48686774_48755724 |
regionname5000 | LHCGR_chr2_48681774_48760724 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 699 | 218 | 16 | 44 | 134 | 7 | 17 | 87 | LHCGR_chr2_48681774_48760724 | LHCGR | MKQRF others(694): Show |
chr2 | 48681774 | 48760724 |
a0002 | 1/1 | 699 | 115 | 58 | 17 | 16 | 3 | 19 | 13 | LHCGR_chr2_48681774_48760724 | LHCGR | MKQRF others(694): Show |
chr2 | 48681774 | 48760724 |
a0003 | 0/0 | 701 | 36 | 15 | 13 | 0 | 2 | 6 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | MKQRF others(696): Show |
chr2 | 48681774 | 48760724 |
a0004 | 0/0 | 699 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | MKQRF others(694): Show |
chr2 | 48681774 | 48760724 |
a0005 | 0/0 | 699 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | MKQRF others(694): Show |
chr2 | 48681774 | 48760724 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2097 | 213 | 16 | 43 | 132 | 7 | 15 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 | ||
a0001c0006 | 0/0 | 2097 | 4 | 0 | 0 | 2 | 0 | 2 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 | ||
a0001c0012 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 | ||
a0002c0002 | 1/1 | 2097 | 108 | 53 | 17 | 15 | 3 | 18 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 | ||
a0002c0005 | 0/0 | 2097 | 4 | 2 | 0 | 1 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 | ||
a0002c0010 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 | ||
a0002c0011 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 | ||
a0003c0003 | 0/0 | 2103 | 17 | 8 | 6 | 0 | 2 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2098): Show |
chr2 | 48681774 | 48760724 | ||
a0003c0004 | 0/0 | 2103 | 15 | 3 | 7 | 0 | 0 | 5 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2098): Show |
chr2 | 48681774 | 48760724 | ||
a0003c0008 | 0/0 | 2103 | 3 | 3 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2098): Show |
chr2 | 48681774 | 48760724 | ||
a0003c0013 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2098): Show |
chr2 | 48681774 | 48760724 | ||
a0004c0007 | 0/0 | 2097 | 3 | 1 | 2 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 | ||
a0005c0009 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ATGAA others(2092): Show |
chr2 | 48681774 | 48760724 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3076 | 208 | 15 | 42 | 129 | 7 | 15 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0001c0001t0006 | 0/0 | 3075 | 3 | 0 | 0 | 3 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3070): Show |
chr2 | 48681774 | 48760724 |
a0001c0001t0007 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0001c0001t0009 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0001c0006t0001 | 0/0 | 3076 | 4 | 0 | 0 | 2 | 0 | 2 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0001c0012t0001 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0002t0001 | 1/0 | 3076 | 32 | 22 | 3 | 0 | 1 | 5 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0002t0002 | 0/1 | 3076 | 46 | 2 | 13 | 15 | 2 | 13 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0002t0003 | 0/0 | 3076 | 13 | 12 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0002t0004 | 0/0 | 3076 | 11 | 11 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0002t0005 | 0/0 | 3076 | 5 | 5 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0002t0008 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0005t0001 | 0/0 | 3076 | 3 | 2 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0005t0002 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0010t0001 | 0/0 | 3076 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0002c0011t0003 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0003c0003t0001 | 0/0 | 3082 | 4 | 1 | 0 | 0 | 2 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3077): Show |
chr2 | 48681774 | 48760724 |
a0003c0003t0002 | 0/0 | 3082 | 5 | 0 | 5 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3077): Show |
chr2 | 48681774 | 48760724 |
a0003c0003t0003 | 0/0 | 3082 | 5 | 5 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3077): Show |
chr2 | 48681774 | 48760724 |
a0003c0003t0004 | 0/0 | 3082 | 3 | 2 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3077): Show |
chr2 | 48681774 | 48760724 |
a0003c0004t0001 | 0/0 | 3082 | 15 | 3 | 7 | 0 | 0 | 5 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3077): Show |
chr2 | 48681774 | 48760724 |
a0003c0008t0004 | 0/0 | 3082 | 3 | 3 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3077): Show |
chr2 | 48681774 | 48760724 |
a0003c0013t0003 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3077): Show |
chr2 | 48681774 | 48760724 |
a0004c0007t0003 | 0/0 | 3076 | 3 | 1 | 2 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
a0005c0009t0004 | 0/0 | 3076 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | ACTCA others(3071): Show |
chr2 | 48681774 | 48760724 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0006t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0006t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0001c0012t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0242 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0308 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0002t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0005t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0005t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0010t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0010t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0002c0011t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0003t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0004t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0008t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0008t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0003c0013t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0004c0007t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0004c0007t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0004c0007t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0005c0009t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
a0005c0009t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0237 | EUR | GBR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | FIN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00639 | hp2 | a0003 | c0004 | t0001 | g0336 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00733 | hp1 | a0003 | c0004 | t0001 | g0345 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0268 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0322 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01069 | hp1 | a0003 | c0003 | t0002 | g0347 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01070 | hp2 | a0004 | c0007 | t0003 | g0316 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01071 | hp2 | a0003 | c0003 | t0002 | g0346 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0310 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0191 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0284 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0281 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01168 | hp2 | a0003 | c0004 | t0001 | g0332 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01169 | hp1 | a0003 | c0004 | t0001 | g0351 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01175 | hp2 | a0003 | c0004 | t0001 | g0339 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0112 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01243 | hp2 | a0003 | c0003 | t0004 | g0342 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0167 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01256 | hp1 | a0003 | c0003 | t0002 | g0354 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01257 | hp1 | a0003 | c0003 | t0002 | g0355 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01261 | hp1 | a0003 | c0004 | t0001 | g0335 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01496 | hp2 | a0003 | c0004 | t0001 | g0356 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01515 | hp2 | a0003 | c0003 | t0001 | g0357 | EUR | IBS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01517 | hp1 | a0003 | c0003 | t0001 | g0330 | EUR | IBS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01891 | hp1 | a0002 | c0002 | t0003 | g0097 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01891 | hp2 | a0002 | c0002 | t0004 | g0078 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0085 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01952 | hp1 | a0001 | c0001 | t0009 | g0217 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01952 | hp2 | a0003 | c0003 | t0002 | g0340 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01975 | hp1 | a0001 | c0012 | t0001 | g0023 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0179 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0323 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02055 | hp2 | a0005 | c0009 | t0004 | g0099 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02145 | hp1 | a0002 | c0002 | t0005 | g0067 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02258 | hp1 | a0002 | c0010 | t0001 | g0211 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0115 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0358 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0297 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0109 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0223 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02602 | hp2 | a0001 | c0006 | t0001 | g0225 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02615 | hp2 | a0003 | c0013 | t0003 | g0341 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02622 | hp1 | a0003 | c0003 | t0003 | g0331 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02622 | hp2 | a0002 | c0002 | t0004 | g0232 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02630 | hp1 | a0002 | c0002 | t0005 | g0250 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02647 | hp1 | a0002 | c0002 | t0004 | g0005 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02647 | hp2 | a0002 | c0002 | t0005 | g0081 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02683 | hp1 | a0003 | c0004 | t0001 | g0337 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0229 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0311 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02698 | hp2 | a0003 | c0004 | t0001 | g0359 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02723 | hp2 | a0002 | c0002 | t0003 | g0293 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02809 | hp1 | a0002 | c0002 | t0003 | g0065 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02818 | hp1 | a0002 | c0002 | t0003 | g0064 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02895 | hp2 | a0003 | c0004 | t0001 | g0352 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0208 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02896 | hp2 | a0002 | c0002 | t0005 | g0326 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0128 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02922 | hp1 | a0003 | c0003 | t0003 | g0348 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02922 | hp2 | a0002 | c0002 | t0004 | g0068 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02965 | hp1 | a0003 | c0003 | t0004 | g0338 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02965 | hp2 | a0002 | c0002 | t0004 | g0074 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02970 | hp1 | a0002 | c0002 | t0004 | g0210 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02976 | hp1 | a0002 | c0005 | t0001 | g0206 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02976 | hp2 | a0002 | c0002 | t0004 | g0080 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0200 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03017 | hp2 | a0003 | c0004 | t0001 | g0333 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03041 | hp2 | a0003 | c0004 | t0001 | g0328 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03098 | hp1 | a0002 | c0011 | t0003 | g0249 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03098 | hp2 | a0002 | c0005 | t0001 | g0066 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03130 | hp2 | a0003 | c0004 | t0001 | g0344 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03139 | hp1 | a0003 | c0008 | t0004 | g0012 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03139 | hp2 | a0002 | c0002 | t0008 | g0098 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03209 | hp1 | a0002 | c0002 | t0004 | g0294 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03225 | hp1 | a0003 | c0008 | t0004 | g0361 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03225 | hp2 | a0002 | c0002 | t0005 | g0213 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03453 | hp1 | a0003 | c0003 | t0003 | g0360 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0170 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03486 | hp2 | a0003 | c0008 | t0004 | g0012 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03516 | hp1 | a0002 | c0002 | t0004 | g0189 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03540 | hp2 | a0002 | c0010 | t0001 | g0212 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0315 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03688 | hp1 | a0002 | c0005 | t0001 | g0148 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03704 | hp1 | a0003 | c0004 | t0001 | g0349 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0324 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03831 | hp2 | a0003 | c0003 | t0001 | g0353 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04115 | hp1 | a0001 | c0006 | t0001 | g0151 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0325 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04184 | hp1 | a0003 | c0004 | t0001 | g0350 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0276 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0149 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0161 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0307 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0145 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0009 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18522 | hp1 | a0003 | c0003 | t0003 | g0343 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18906 | hp1 | a0002 | c0002 | t0003 | g0171 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18940 | hp1 | a0001 | c0006 | t0001 | g0288 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18995 | hp1 | a0002 | c0005 | t0002 | g0144 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19011 | hp1 | a0001 | c0006 | t0001 | g0260 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19030 | hp1 | a0003 | c0003 | t0003 | g0329 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19030 | hp2 | a0005 | c0009 | t0004 | g0069 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19086 | hp1 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0295 | AFR | ASW | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0302 | EUR | TSI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0313 | EUR | TSI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | GIH | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | GIH | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01123 | hp1 | a0004 | c0007 | t0003 | g0047 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02486 | hp1 | a0002 | c0002 | t0003 | g0245 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0317 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG02559 | hp2 | a0003 | c0003 | t0004 | g0334 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03471 | hp1 | a0002 | c0002 | t0004 | g0076 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0110 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG06807 | hp1 | a0002 | c0002 | t0004 | g0005 | AFR | USA | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
HG06807 | hp2 | a0002 | c0002 | t0003 | g0262 | AFR | USA | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | USA | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA20300 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | USA | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA21309 | hp1 | a0004 | c0007 | t0003 | g0296 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0308 | REF | REF | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0242 | REF | REF | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48694236 | T | C | 2 | a0001 a0003 |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
missense_variant | MODERATE | c.935A>G | p.Asn312Ser | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/11 | 988/3076 | 935/2100 | 312/699 | chr2 | 48694236 | |||
chr2:48694299 | T | C | 1 | a0004 | 3 | HG01070.hp2 HG01123.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.872A>G | p.Asn291Ser | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/11 | 925/3076 | 872/2100 | 291/699 | chr2 | 48694299 | |||
chr2:48709006 | C | T | 2 | a0003 a0005 |
5 | HG02055.hp2 HG03139.hp1 HG03225.hp1 others(2): Show |
missense_variant | MODERATE | c.622G>A | p.Val208Ile | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/11 | 675/3076 | 622/2100 | 208/699 | chr2 | 48709006 | |||
chr2:48755616 | G | GGCTGCA | 1 | a0003 | 36 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(33): Show |
conservative_inframe_insertion | MODERATE | c.50_55dupTGCAGC | p.Leu17_Gln18dup | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/11 | 108/3076 | 55/2100 | 19/699 | chr2 | 48755616 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48687928 | A | G | 1 | a0002c0011 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1869T>C | p.Tyr623Tyr | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 1922/3076 | 1869/2100 | 623/699 | chr2 | 48687928 | |||
chr2:48688684 | A | G | 1 | a0002c0010 | 2 | HG02258.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.1113T>C | p.Ile371Ile | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 1166/3076 | 1113/2100 | 371/699 | chr2 | 48688684 | |||
chr2:48688732 | A | G | 4 | a0001c0001 a0001c0012 a0002c0005 others(1): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
synonymous_variant | LOW | c.1065T>C | p.Asp355Asp | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 1118/3076 | 1065/2100 | 355/699 | chr2 | 48688732 | |||
chr2:48698710 | T | C | 1 | a0001c0012 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.771A>G | p.Lys257Lys | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/11 | 824/3076 | 771/2100 | 257/699 | chr2 | 48698710 | |||
chr2:48723654 | C | T | 1 | a0003c0013 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.426G>A | p.Thr142Thr | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 5/11 | 479/3076 | 426/2100 | 142/699 | chr2 | 48723654 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48687013 | T | A | 1 | a0001c0001t0009 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*684A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 684 | chr2 | 48687013 | ||||||
chr2:48687169 | A | G | 5 | a0002c0002t0004 a0002c0002t0008 a0003c0003t0004 others(2): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*528T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 528 | chr2 | 48687169 | ||||||
chr2:48687207 | T | G | 1 | a0002c0002t0008 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 490 | chr2 | 48687207 | ||||||
chr2:48687337 | C | T | 5 | a0002c0002t0004 a0002c0002t0008 a0003c0003t0004 others(2): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*360G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 360 | chr2 | 48687337 | ||||||
chr2:48687415 | GT | G | 1 | a0001c0001t0006 | 3 | NA19066.hp1 NA19086.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*281delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 281 | chr2 | 48687415 | ||||||
chr2:48687476 | C | G | 4 | a0002c0002t0002 a0002c0002t0005 a0002c0005t0002 others(1): Show |
56 | HG00099.hp2 HG00544.hp2 HG00733.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*221G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 221 | chr2 | 48687476 | ||||||
chr2:48687549 | A | G | 5 | a0002c0002t0003 a0002c0011t0003 a0003c0003t0003 others(2): Show |
23 | HG01070.hp2 HG01123.hp1 HG01243.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*148T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 148 | chr2 | 48687549 | ||||||
chr2:48687566 | G | A | 1 | a0002c0002t0005 | 5 | HG02145.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*131C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 131 | chr2 | 48687566 | ||||||
chr2:48687675 | A | C | 1 | a0001c0001t0007 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 22 | chr2 | 48687675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48688962 | C | T | 18 | a0002c0002t0004g0005 a0002c0002t0004g0068 a0002c0002t0004g0074 others(15): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.948-113G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48688962 | |||||||
chr2:48689059 | A | G | 1 | a0002c0002t0001g0082 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.948-210T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689059 | |||||||
chr2:48689082 | T | C | 1 | a0001c0012t0001g0023 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.948-233A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689082 | |||||||
chr2:48689090 | TATATATA others(11): Show |
T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0280 |
2 | HG02074.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.948-259_948-242del others(18): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689090 | |||||||
chr2:48689172 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.948-323G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689172 | |||||||
chr2:48689184 | C | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.948-335G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689184 | |||||||
chr2:48689185 | A | G | 12 | a0002c0002t0001g0082 a0002c0002t0001g0092 a0002c0002t0001g0229 others(9): Show |
12 | HG00642.hp2 HG01361.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-336T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689185 | |||||||
chr2:48689315 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.948-466T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689315 | |||||||
chr2:48689427 | G | C | 2 | a0002c0002t0003g0245 a0002c0002t0003g0262 |
2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.948-578C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689427 | |||||||
chr2:48689466 | A | T | 1 | a0002c0002t0001g0325 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.948-617T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689466 | |||||||
chr2:48689493 | C | T | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(327): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.948-644G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689493 | |||||||
chr2:48689676 | C | T | 1 | a0002c0002t0002g0164 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.948-827G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689676 | |||||||
chr2:48689683 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.948-834T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689683 | |||||||
chr2:48689725 | T | C | 50 | a0002c0002t0002g0009 a0002c0002t0002g0020 a0002c0002t0002g0038 others(47): Show |
51 | HG00099.hp2 HG00544.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.948-876A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689725 | |||||||
chr2:48689738 | C | T | 3 | a0001c0001t0001g0163 a0002c0002t0002g0150 a0003c0003t0002g0354 |
3 | HG00609.hp1 HG01256.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.948-889G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689738 | |||||||
chr2:48689933 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.948-1084G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689933 | |||||||
chr2:48689950 | G | A | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(327): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.948-1101C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689950 | |||||||
chr2:48690004 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0255 a0001c0001t0001g0279 others(1): Show |
4 | HG00741.hp2 NA18998.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-1155G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690004 | |||||||
chr2:48690005 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0026 |
2 | NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.948-1156C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690005 | |||||||
chr2:48690037 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.948-1188C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690037 | |||||||
chr2:48690101 | G | A | 5 | a0002c0002t0005g0067 a0002c0002t0005g0081 a0002c0002t0005g0213 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-1252C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690101 | |||||||
chr2:48690158 | C | G | 1 | a0002c0002t0001g0243 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.948-1309G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690158 | |||||||
chr2:48690158 | C | T | 18 | a0002c0002t0004g0005 a0002c0002t0004g0068 a0002c0002t0004g0074 others(15): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.948-1309G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690158 | |||||||
chr2:48690669 | G | A | 2 | a0005c0009t0004g0069 a0005c0009t0004g0099 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.948-1820C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690669 | |||||||
chr2:48690689 | A | G | 1 | a0002c0002t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.948-1840T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690689 | |||||||
chr2:48690703 | A | G | 12 | a0002c0002t0001g0082 a0002c0002t0001g0092 a0002c0002t0001g0229 others(9): Show |
12 | HG00642.hp2 HG01361.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-1854T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690703 | |||||||
chr2:48690814 | C | A | 1 | a0002c0002t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.948-1965G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690814 | |||||||
chr2:48690884 | G | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.948-2035C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690884 | |||||||
chr2:48691003 | C | T | 1 | a0002c0002t0002g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.948-2154G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691003 | |||||||
chr2:48691119 | T | C | 2 | a0004c0007t0003g0047 a0004c0007t0003g0316 |
2 | HG01070.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.948-2270A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691119 | |||||||
chr2:48691402 | G | A | 7 | a0002c0002t0002g0087 a0002c0002t0002g0147 a0002c0002t0002g0155 others(4): Show |
7 | HG02129.hp2 NA18948.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-2553C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691402 | |||||||
chr2:48691476 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.948-2627T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691476 | |||||||
chr2:48691517 | A | G | 2 | a0001c0001t0001g0301 a0001c0001t0001g0321 |
2 | NA18974.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.948-2668T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691517 | |||||||
chr2:48691574 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0304 |
2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.947+2650C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691574 | |||||||
chr2:48691656 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.947+2568C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691656 | |||||||
chr2:48691769 | T | C | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.947+2455A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691769 | |||||||
chr2:48691818 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0007g0115 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.947+2406G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691818 | |||||||
chr2:48691845 | C | CA | 15 | a0001c0001t0001g0049 a0001c0001t0001g0086 a0001c0001t0001g0101 others(12): Show |
15 | HG01081.hp2 HG01099.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.947+2378dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691845 | |||||||
chr2:48691845 | CA | C | 30 | a0001c0001t0001g0039 a0001c0001t0001g0162 a0001c0001t0001g0238 others(27): Show |
30 | HG00738.hp2 HG01070.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.947+2378delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691845 | |||||||
chr2:48691845 | CAA | C | 16 | a0002c0002t0004g0005 a0002c0002t0004g0068 a0002c0002t0004g0074 others(13): Show |
18 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.947+2377_947+2378d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691845 | |||||||
chr2:48691845 | CAAA | C | 31 | a0002c0002t0001g0016 a0002c0002t0001g0030 a0002c0002t0001g0037 others(28): Show |
31 | HG00642.hp2 HG01109.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.947+2376_947+2378d others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691845 | |||||||
chr2:48691877 | C | T | 1 | a0002c0002t0002g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.947+2347G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691877 | |||||||
chr2:48692149 | C | T | 2 | a0002c0002t0002g0200 a0002c0002t0002g0311 |
2 | HG02698.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.947+2075G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692149 | |||||||
chr2:48692270 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.947+1954T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692270 | |||||||
chr2:48692360 | T | C | 14 | a0001c0001t0001g0033 a0001c0001t0001g0062 a0001c0001t0001g0088 others(11): Show |
14 | HG00558.hp2 HG00609.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.947+1864A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692360 | |||||||
chr2:48692458 | T | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.947+1766A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692458 | |||||||
chr2:48692516 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.947+1708G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692516 | |||||||
chr2:48692641 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0006g0126 |
2 | NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.947+1583G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692641 | |||||||
chr2:48692925 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | HG02027.hp2 HG02165.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+1299T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692925 | |||||||
chr2:48693124 | C | T | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.947+1100G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48693124 | |||||||
chr2:48693802 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.947+422T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48693802 | |||||||
chr2:48694572 | A | G | 2 | a0002c0005t0001g0066 a0002c0005t0001g0206 |
2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.867-268T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48694572 | |||||||
chr2:48694982 | C | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.867-678G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48694982 | |||||||
chr2:48695038 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.867-734A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695038 | |||||||
chr2:48695049 | A | G | 2 | a0002c0002t0001g0139 a0002c0002t0001g0204 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.867-745T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695049 | |||||||
chr2:48695275 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
12 | NA18944.hp1 NA18952.hp1 NA18962.hp2 others(9): Show |
intron_variant | MODIFIER | c.867-971G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695275 | |||||||
chr2:48695414 | T | C | 1 | a0002c0002t0003g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.867-1110A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695414 | |||||||
chr2:48695422 | C | T | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.867-1118G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695422 | |||||||
chr2:48695445 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.867-1141T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695445 | |||||||
chr2:48695446 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.867-1142G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695446 | |||||||
chr2:48695564 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.867-1260T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695564 | |||||||
chr2:48695884 | C | G | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.867-1580G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695884 | |||||||
chr2:48695926 | T | C | 357 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(354): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.867-1622A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695926 | |||||||
chr2:48696015 | A | C | 17 | a0002c0002t0003g0014 a0002c0002t0003g0064 a0002c0002t0003g0065 others(14): Show |
17 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.867-1711T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696015 | |||||||
chr2:48696141 | C | T | 4 | a0001c0001t0001g0173 a0001c0001t0001g0187 a0001c0001t0001g0220 others(1): Show |
4 | HG00438.hp2 NA18947.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.867-1837G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696141 | |||||||
chr2:48696170 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.867-1866T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696170 | |||||||
chr2:48696264 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
7 | HG01099.hp2 NA18945.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.867-1960T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696264 | |||||||
chr2:48696330 | A | C | 1 | a0002c0002t0002g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.867-2026T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696330 | |||||||
chr2:48696388 | A | G | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.867-2084T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696388 | |||||||
chr2:48696396 | G | T | 19 | a0002c0002t0001g0234 a0002c0002t0004g0005 a0002c0002t0004g0068 others(16): Show |
21 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.867-2092C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696396 | |||||||
chr2:48696403 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.867-2099G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696403 | |||||||
chr2:48696408 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.867-2104G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696408 | |||||||
chr2:48696483 | G | T | 5 | a0002c0002t0005g0067 a0002c0002t0005g0081 a0002c0002t0005g0213 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.866+2132C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696483 | |||||||
chr2:48696595 | A | C | 12 | a0002c0002t0001g0082 a0002c0002t0001g0092 a0002c0002t0001g0229 others(9): Show |
12 | HG00642.hp2 HG01361.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.866+2020T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696595 | |||||||
chr2:48696687 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.866+1928C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696687 | |||||||
chr2:48696711 | T | G | 4 | a0002c0002t0003g0110 a0002c0002t0003g0112 a0003c0003t0003g0329 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.866+1904A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696711 | |||||||
chr2:48696788 | T | A | 1 | a0002c0002t0001g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.866+1827A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696788 | |||||||
chr2:48696832 | C | CA | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.866+1782dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696832 | |||||||
chr2:48696892 | C | T | 23 | a0002c0002t0001g0234 a0002c0002t0003g0014 a0002c0002t0003g0064 others(20): Show |
23 | HG01070.hp2 HG01123.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.866+1723G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696892 | |||||||
chr2:48696909 | C | A | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.866+1706G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696909 | |||||||
chr2:48696952 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(318): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.866+1663G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696952 | |||||||
chr2:48697063 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.866+1552G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697063 | |||||||
chr2:48697099 | C | T | 1 | a0002c0002t0001g0243 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.866+1516G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697099 | |||||||
chr2:48697174 | T | G | 357 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(354): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.866+1441A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697174 | |||||||
chr2:48697337 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.866+1278G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697337 | |||||||
chr2:48697682 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0025 others(73): Show |
78 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.866+933T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697682 | |||||||
chr2:48697684 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0096 others(3): Show |
7 | HG02015.hp2 HG02056.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.866+931A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697684 | |||||||
chr2:48697690 | A | T | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.866+925T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697690 | |||||||
chr2:48697737 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0091 a0001c0001t0001g0093 others(1): Show |
4 | HG01106.hp1 HG01255.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+878G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697737 | |||||||
chr2:48698012 | A | G | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.866+603T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698012 | |||||||
chr2:48698013 | C | T | 1 | a0003c0004t0001g0328 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.866+602G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698013 | |||||||
chr2:48698033 | C | T | 2 | a0002c0002t0001g0139 a0002c0002t0001g0204 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.866+582G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698033 | |||||||
chr2:48698051 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.866+564C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698051 | |||||||
chr2:48698552 | C | G | 14 | a0001c0001t0001g0184 a0001c0001t0001g0240 a0001c0001t0001g0312 others(11): Show |
14 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.866+63G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698552 | |||||||
chr2:48698590 | G | A | 2 | a0003c0003t0001g0353 a0003c0003t0001g0358 |
2 | HG02280.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.866+25C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698590 | |||||||
chr2:48698597 | C | G | 1 | a0003c0008t0004g0361 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.866+18G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698597 | |||||||
chr2:48698607 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(238): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
splice_region_variant&intron_variant | LOW | c.866+8G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698607 | |||||||
chr2:48698847 | AT | A | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(349): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.681-48delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48698847 | |||||||
chr2:48698993 | T | C | 8 | a0001c0001t0001g0158 a0001c0001t0001g0231 a0001c0001t0001g0318 others(5): Show |
8 | HG00140.hp2 HG01257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.681-193A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48698993 | |||||||
chr2:48698999 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.681-199C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48698999 | |||||||
chr2:48699043 | G | C | 357 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(354): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.681-243C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699043 | |||||||
chr2:48699170 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0096 a0001c0001t0001g0259 others(2): Show |
6 | HG02015.hp2 HG02056.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-370T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699170 | |||||||
chr2:48699282 | C | G | 2 | a0001c0001t0001g0263 a0002c0002t0001g0234 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.681-482G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699282 | |||||||
chr2:48699302 | C | G | 1 | a0001c0001t0001g0321 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.681-502G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699302 | |||||||
chr2:48699458 | C | G | 1 | a0003c0008t0004g0361 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.681-658G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699458 | |||||||
chr2:48699649 | A | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0233 others(21): Show |
28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.681-849T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699649 | |||||||
chr2:48699664 | TAATGCAT others(26): Show |
T | 1 | a0001c0006t0001g0151 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.681-897_681-865del others(33): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699664 | |||||||
chr2:48699873 | C | T | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.681-1073G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699873 | |||||||
chr2:48700024 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.681-1224A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700024 | |||||||
chr2:48700059 | C | T | 3 | a0002c0002t0004g0068 a0003c0003t0004g0334 a0003c0003t0004g0338 |
3 | HG02559.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.681-1259G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700059 | |||||||
chr2:48700090 | G | T | 1 | a0002c0002t0002g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.681-1290C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700090 | |||||||
chr2:48700107 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0057 others(66): Show |
73 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.681-1307T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700107 | |||||||
chr2:48700136 | A | G | 1 | a0002c0002t0001g0297 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.681-1336T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700136 | |||||||
chr2:48700364 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.681-1564C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700364 | |||||||
chr2:48700556 | C | T | 8 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0061 others(5): Show |
8 | HG00642.hp1 HG02273.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.681-1756G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700556 | |||||||
chr2:48700568 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.681-1768A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700568 | |||||||
chr2:48700737 | AGACCCCT others(35): Show |
A | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-1979_681-1938d others(44): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700737 | |||||||
chr2:48700898 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.681-2098C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700898 | |||||||
chr2:48701160 | T | A | 4 | a0003c0008t0004g0012 a0003c0008t0004g0361 a0005c0009t0004g0069 others(1): Show |
5 | HG02055.hp2 HG03139.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-2360A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701160 | |||||||
chr2:48701394 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0057 others(65): Show |
72 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.681-2594G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701394 | |||||||
chr2:48701460 | T | C | 1 | a0003c0004t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.681-2660A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701460 | |||||||
chr2:48701503 | A | G | 54 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0028 others(51): Show |
55 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.681-2703T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701503 | |||||||
chr2:48701544 | A | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0233 others(21): Show |
28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.681-2744T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701544 | |||||||
chr2:48702010 | T | G | 2 | a0003c0003t0002g0346 a0003c0003t0002g0347 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.681-3210A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702010 | |||||||
chr2:48702053 | C | T | 1 | a0002c0002t0002g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.681-3253G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702053 | |||||||
chr2:48702063 | AG | A | 15 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0002c0002t0001g0139 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.681-3264delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702063 | |||||||
chr2:48702068 | G | A | 39 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(36): Show |
39 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.681-3268C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702068 | |||||||
chr2:48702263 | C | CT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0233 others(21): Show |
28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.681-3464dupA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702263 | |||||||
chr2:48702263 | CT | C | 47 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0103 others(44): Show |
47 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.681-3464delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702263 | |||||||
chr2:48702277 | T | A | 1 | a0002c0002t0002g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.681-3477A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702277 | |||||||
chr2:48702282 | A | G | 4 | a0001c0001t0001g0207 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG01358.hp1 HG02970.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-3482T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702282 | |||||||
chr2:48702327 | A | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.681-3527T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702327 | |||||||
chr2:48702357 | G | A | 39 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(36): Show |
39 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.681-3557C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702357 | |||||||
chr2:48702406 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-3606G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702406 | |||||||
chr2:48702407 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-3607A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702407 | |||||||
chr2:48702408 | C | A | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-3608G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702408 | |||||||
chr2:48702424 | C | T | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.681-3624G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702424 | |||||||
chr2:48702425 | G | C | 95 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0052 others(92): Show |
95 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.681-3625C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702425 | |||||||
chr2:48702453 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(36): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-3653G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702453 | |||||||
chr2:48702639 | C | T | 3 | a0001c0001t0001g0118 a0001c0006t0001g0225 a0002c0002t0002g0200 |
3 | HG02300.hp1 HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.681-3839G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702639 | |||||||
chr2:48702798 | C | T | 1 | a0003c0004t0001g0345 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.681-3998G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702798 | |||||||
chr2:48702807 | A | T | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.681-4007T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702807 | |||||||
chr2:48702821 | G | A | 1 | a0002c0010t0001g0212 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.681-4021C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702821 | |||||||
chr2:48702929 | A | G | 2 | a0002c0002t0001g0139 a0002c0002t0001g0204 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.681-4129T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702929 | |||||||
chr2:48703015 | A | G | 1 | a0002c0002t0002g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.681-4215T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703015 | |||||||
chr2:48703074 | T | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0233 others(22): Show |
29 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-4274A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703074 | |||||||
chr2:48703113 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.681-4313C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703113 | |||||||
chr2:48703224 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0233 others(21): Show |
28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.681-4424C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703224 | |||||||
chr2:48703429 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.681-4629G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703429 | |||||||
chr2:48703551 | C | G | 3 | a0001c0001t0001g0263 a0002c0002t0001g0234 a0002c0002t0003g0245 |
3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.681-4751G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703551 | |||||||
chr2:48703681 | C | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.681-4881G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703681 | |||||||
chr2:48703752 | C | T | 5 | a0002c0002t0001g0209 a0002c0002t0001g0244 a0002c0002t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-4952G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703752 | |||||||
chr2:48703753 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.681-4953C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703753 | |||||||
chr2:48703864 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.681-5064T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703864 | |||||||
chr2:48703889 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0096 a0001c0001t0001g0259 others(2): Show |
6 | HG02015.hp2 HG02056.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+5059G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703889 | |||||||
chr2:48703907 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0327 a0002c0002t0002g0161 others(1): Show |
4 | HG01361.hp2 HG02735.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+5041T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703907 | |||||||
chr2:48703915 | C | A | 1 | a0003c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.680+5033G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703915 | |||||||
chr2:48704169 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0233 others(21): Show |
28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.680+4779G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704169 | |||||||
chr2:48704211 | A | G | 1 | a0003c0004t0001g0356 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.680+4737T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704211 | |||||||
chr2:48704261 | C | T | 2 | a0001c0001t0001g0207 a0002c0002t0003g0262 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.680+4687G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704261 | |||||||
chr2:48704301 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0233 others(21): Show |
28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.680+4647A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704301 | |||||||
chr2:48704317 | C | T | 9 | a0001c0001t0001g0075 a0002c0002t0001g0016 a0002c0002t0001g0030 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.680+4631G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704317 | |||||||
chr2:48704318 | G | A | 1 | a0002c0002t0001g0297 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.680+4630C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704318 | |||||||
chr2:48704470 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.680+4478C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704470 | |||||||
chr2:48704518 | C | A | 29 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0104 others(26): Show |
29 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+4430G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704518 | |||||||
chr2:48704571 | G | GTTATTGG others(126): Show |
1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.680+4244_680+4376d others(135): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704571 | |||||||
chr2:48704599 | C | A | 1 | a0001c0001t0001g0230 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.680+4349G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704599 | |||||||
chr2:48704662 | C | G | 1 | a0002c0002t0002g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.680+4286G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704662 | |||||||
chr2:48705037 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.680+3911T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705037 | |||||||
chr2:48705083 | C | T | 3 | a0002c0002t0005g0067 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3865G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705083 | |||||||
chr2:48705084 | A | G | 3 | a0002c0002t0005g0067 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3864T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705084 | |||||||
chr2:48705087 | A | G | 3 | a0002c0002t0005g0067 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3861T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705087 | |||||||
chr2:48705130 | C | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0096 a0001c0001t0001g0199 others(4): Show |
8 | HG00558.hp2 HG02015.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.680+3818G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705130 | |||||||
chr2:48705245 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0041 others(1): Show |
4 | HG00558.hp1 HG02027.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+3703C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705245 | |||||||
chr2:48705408 | T | G | 3 | a0002c0002t0005g0067 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3540A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705408 | |||||||
chr2:48705506 | T | G | 1 | a0002c0002t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.680+3442A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705506 | |||||||
chr2:48705539 | T | G | 3 | a0002c0002t0005g0067 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3409A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705539 | |||||||
chr2:48705590 | T | A | 1 | a0001c0001t0001g0277 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.680+3358A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705590 | |||||||
chr2:48705793 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0221 |
2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.680+3155T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705793 | |||||||
chr2:48705806 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(37): Show |
42 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.680+3142G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705806 | |||||||
chr2:48705809 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.680+3139G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705809 | |||||||
chr2:48705952 | A | G | 3 | a0002c0002t0005g0067 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+2996T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705952 | |||||||
chr2:48705957 | G | A | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.680+2991C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705957 | |||||||
chr2:48706289 | G | A | 3 | a0001c0001t0001g0263 a0002c0002t0001g0234 a0002c0002t0003g0245 |
3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+2659C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706289 | |||||||
chr2:48706354 | A | G | 1 | a0002c0002t0003g0245 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.680+2594T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706354 | |||||||
chr2:48706384 | C | T | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.680+2564G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706384 | |||||||
chr2:48706412 | C | T | 26 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0104 others(23): Show |
26 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.680+2536G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706412 | |||||||
chr2:48706534 | C | T | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.680+2414G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706534 | |||||||
chr2:48706665 | T | C | 5 | a0001c0001t0001g0287 a0003c0003t0002g0346 a0003c0003t0002g0347 others(2): Show |
5 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+2283A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706665 | |||||||
chr2:48706705 | C | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0104 others(29): Show |
32 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.680+2243G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706705 | |||||||
chr2:48706737 | G | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
232 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.680+2211C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706737 | |||||||
chr2:48706751 | G | A | 26 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0104 others(23): Show |
26 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.680+2197C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706751 | |||||||
chr2:48706762 | C | T | 21 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0001c0001t0001g0292 others(18): Show |
21 | HG00738.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.680+2186G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706762 | |||||||
chr2:48706788 | C | T | 39 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(36): Show |
39 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.680+2160G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706788 | |||||||
chr2:48706814 | C | G | 2 | a0002c0002t0002g0310 a0003c0003t0002g0354 |
2 | HG01081.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.680+2134G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706814 | |||||||
chr2:48706873 | C | G | 20 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0002c0002t0001g0139 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.680+2075G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706873 | |||||||
chr2:48706895 | G | A | 32 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0104 others(29): Show |
32 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.680+2053C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706895 | |||||||
chr2:48706906 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.680+2042A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706906 | |||||||
chr2:48706967 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0121 a0001c0001t0001g0301 |
3 | HG00438.hp1 NA18974.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.680+1981G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706967 | |||||||
chr2:48707069 | G | A | 3 | a0002c0002t0005g0067 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+1879C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707069 | |||||||
chr2:48707192 | G | A | 38 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(35): Show |
38 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.680+1756C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707192 | |||||||
chr2:48707196 | T | C | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(353): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.680+1752A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707196 | |||||||
chr2:48707196 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.680+1752A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707196 | |||||||
chr2:48707245 | C | G | 3 | a0001c0001t0001g0263 a0002c0002t0001g0234 a0002c0002t0003g0245 |
3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+1703G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707245 | |||||||
chr2:48707280 | G | A | 3 | a0001c0001t0001g0263 a0002c0002t0001g0234 a0002c0002t0003g0245 |
3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+1668C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707280 | |||||||
chr2:48707317 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0006g0126 |
3 | HG02074.hp2 NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.680+1631A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707317 | |||||||
chr2:48707342 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.680+1606C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707342 | |||||||
chr2:48707400 | C | G | 1 | a0001c0001t0001g0319 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.680+1548G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707400 | |||||||
chr2:48707420 | CTG | C | 33 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0104 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.680+1526_680+1527d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707420 | |||||||
chr2:48707484 | T | C | 72 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0052 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.680+1464A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707484 | |||||||
chr2:48707490 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.680+1458G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707490 | |||||||
chr2:48707683 | T | C | 5 | a0001c0001t0001g0240 a0001c0001t0001g0314 a0002c0002t0002g0109 others(2): Show |
5 | HG00280.hp1 HG01981.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+1265A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707683 | |||||||
chr2:48707733 | A | G | 2 | a0001c0001t0001g0207 a0002c0002t0003g0262 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.680+1215T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707733 | |||||||
chr2:48707995 | G | A | 2 | a0002c0005t0001g0066 a0002c0011t0003g0249 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.680+953C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707995 | |||||||
chr2:48708002 | C | G | 22 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0001c0001t0001g0292 others(19): Show |
22 | HG00738.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.680+946G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708002 | |||||||
chr2:48708050 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.680+898G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708050 | |||||||
chr2:48708071 | C | T | 72 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0052 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.680+877G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708071 | |||||||
chr2:48708092 | C | A | 72 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0052 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.680+856G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708092 | |||||||
chr2:48708109 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.680+839C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708109 | |||||||
chr2:48708152 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
5 | HG01123.hp2 HG01192.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+796C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708152 | |||||||
chr2:48708181 | T | G | 1 | a0002c0002t0002g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.680+767A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708181 | |||||||
chr2:48708187 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.680+761G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708187 | |||||||
chr2:48708253 | C | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
296 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.680+695G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708253 | |||||||
chr2:48708475 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.680+473C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708475 | |||||||
chr2:48708484 | A | C | 1 | a0001c0001t0001g0304 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.680+464T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708484 | |||||||
chr2:48708548 | CCA | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(49): Show |
54 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.680+398_680+399del others(2): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708548 | |||||||
chr2:48708548 | CCACA | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(298): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.680+396_680+399del others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708548 | |||||||
chr2:48708548 | CCACACA | C | 4 | a0002c0002t0001g0297 a0002c0002t0005g0067 a0002c0002t0005g0250 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+394_680+399del others(6): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708548 | |||||||
chr2:48708668 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.680+280G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708668 | |||||||
chr2:48708710 | C | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0111 others(43): Show |
50 | HG00738.hp1 HG01243.hp1 HG01361.hp1 others(47): Show |
intron_variant | MODIFIER | c.680+238G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708710 | |||||||
chr2:48708791 | T | C | 50 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0042 others(47): Show |
51 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.680+157A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708791 | |||||||
chr2:48708828 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0006g0126 |
2 | NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.680+120G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708828 | |||||||
chr2:48708867 | G | A | 32 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0104 others(29): Show |
32 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.680+81C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708867 | |||||||
chr2:48708876 | G | A | 1 | a0002c0002t0003g0170 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.680+72C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708876 | |||||||
chr2:48709290 | C | T | 3 | a0002c0002t0003g0171 a0002c0002t0003g0293 a0002c0011t0003g0249 |
3 | HG02723.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.606-268G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709290 | |||||||
chr2:48709291 | C | G | 1 | a0002c0002t0005g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.606-269G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709291 | |||||||
chr2:48709312 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0096 a0001c0001t0001g0199 others(6): Show |
10 | HG00558.hp2 HG02015.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.606-290T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709312 | |||||||
chr2:48709320 | A | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.606-298T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709320 | |||||||
chr2:48709450 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.606-428A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709450 | |||||||
chr2:48709453 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.606-431A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709453 | |||||||
chr2:48709621 | C | T | 5 | a0002c0002t0001g0209 a0002c0002t0001g0244 a0002c0002t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.606-599G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709621 | |||||||
chr2:48709720 | AG | A | 11 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0267 others(8): Show |
11 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.606-699delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709720 | |||||||
chr2:48709778 | ATCTGG | A | 3 | a0001c0001t0001g0254 a0001c0001t0001g0264 a0002c0002t0002g0324 |
3 | HG03654.hp2 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.606-761_606-757del others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709778 | |||||||
chr2:48709794 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.606-772G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709794 | |||||||
chr2:48709944 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.606-922C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709944 | |||||||
chr2:48709945 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.606-923G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709945 | |||||||
chr2:48709974 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(73): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.606-952C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709974 | |||||||
chr2:48710015 | C | T | 47 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0042 others(44): Show |
48 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.606-993G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710015 | |||||||
chr2:48710084 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0006g0126 |
2 | NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.606-1062A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710084 | |||||||
chr2:48710210 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(73): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.606-1188C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710210 | |||||||
chr2:48710329 | A | G | 1 | a0002c0002t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.606-1307T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710329 | |||||||
chr2:48710437 | G | A | 24 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0117 others(21): Show |
24 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.606-1415C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710437 | |||||||
chr2:48710475 | C | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
140 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.606-1453G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710475 | |||||||
chr2:48710632 | A | C | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.606-1610T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710632 | |||||||
chr2:48710638 | C | G | 3 | a0001c0001t0001g0263 a0002c0002t0001g0234 a0002c0002t0003g0245 |
3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.606-1616G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710638 | |||||||
chr2:48710684 | T | G | 66 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0052 others(63): Show |
66 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.606-1662A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710684 | |||||||
chr2:48710773 | T | C | 1 | a0003c0004t0001g0344 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.606-1751A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710773 | |||||||
chr2:48710800 | G | T | 15 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0002c0002t0001g0139 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.606-1778C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710800 | |||||||
chr2:48710844 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.606-1822C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710844 | |||||||
chr2:48710901 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.606-1879G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710901 | |||||||
chr2:48710989 | C | A | 1 | a0001c0001t0001g0306 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.606-1967G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710989 | |||||||
chr2:48711116 | G | A | 5 | a0001c0001t0001g0287 a0003c0003t0002g0346 a0003c0003t0002g0347 others(2): Show |
5 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.606-2094C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711116 | |||||||
chr2:48711202 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.606-2180T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711202 | |||||||
chr2:48711217 | C | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(198): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.606-2195G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711217 | |||||||
chr2:48711218 | G | T | 2 | a0002c0002t0002g0310 a0003c0003t0002g0354 |
2 | HG01081.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.606-2196C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711218 | |||||||
chr2:48711221 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0269 |
2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.606-2199G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711221 | |||||||
chr2:48711523 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.605+2463G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711523 | |||||||
chr2:48711552 | C | T | 209 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.605+2434G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711552 | |||||||
chr2:48711554 | T | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(79): Show |
86 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.605+2432A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711554 | |||||||
chr2:48711582 | T | A | 159 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
165 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.605+2404A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711582 | |||||||
chr2:48711654 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(164): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.605+2332A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711654 | |||||||
chr2:48711699 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(38): Show |
43 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.605+2287G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711699 | |||||||
chr2:48711768 | A | C | 1 | a0001c0001t0001g0182 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.605+2218T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711768 | |||||||
chr2:48711957 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.605+2029T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711957 | |||||||
chr2:48711994 | G | A | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.605+1992C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711994 | |||||||
chr2:48712038 | A | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.605+1948T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712038 | |||||||
chr2:48712282 | G | T | 1 | a0002c0002t0003g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.605+1704C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712282 | |||||||
chr2:48712407 | A | G | 6 | a0002c0002t0001g0082 a0002c0002t0001g0229 a0003c0003t0001g0330 others(3): Show |
6 | HG01361.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.605+1579T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712407 | |||||||
chr2:48712413 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(69): Show |
74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.605+1573C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712413 | |||||||
chr2:48712418 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.605+1568G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712418 | |||||||
chr2:48712506 | G | A | 3 | a0001c0001t0001g0207 a0002c0002t0001g0246 a0002c0002t0003g0262 |
3 | HG02970.hp2 HG04204.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.605+1480C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712506 | |||||||
chr2:48712560 | C | T | 1 | a0003c0004t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.605+1426G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712560 | |||||||
chr2:48712571 | C | G | 1 | a0002c0002t0005g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.605+1415G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712571 | |||||||
chr2:48712589 | T | G | 2 | a0002c0002t0002g0273 a0002c0005t0002g0144 |
2 | NA18995.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.605+1397A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712589 | |||||||
chr2:48712590 | A | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(69): Show |
74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.605+1396T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712590 | |||||||
chr2:48712603 | A | G | 54 | a0001c0001t0001g0039 a0001c0001t0001g0075 a0001c0001t0001g0156 others(51): Show |
54 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.605+1383T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712603 | |||||||
chr2:48712723 | C | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(69): Show |
74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.605+1263G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712723 | |||||||
chr2:48712781 | T | C | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.605+1205A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712781 | |||||||
chr2:48712814 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(51): Show |
56 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.605+1172A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712814 | |||||||
chr2:48712858 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.605+1128T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712858 | |||||||
chr2:48712934 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0071 others(46): Show |
52 | HG00099.hp2 HG00738.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.605+1052T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712934 | |||||||
chr2:48713007 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(283): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.605+979G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713007 | |||||||
chr2:48713016 | G | A | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.605+970C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713016 | |||||||
chr2:48713074 | A | T | 2 | a0002c0002t0002g0322 a0002c0002t0002g0323 |
2 | HG00735.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.605+912T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713074 | |||||||
chr2:48713083 | G | A | 2 | a0002c0002t0002g0268 a0002c0002t0002g0281 |
2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.605+903C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713083 | |||||||
chr2:48713161 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
152 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.605+825G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713161 | |||||||
chr2:48713227 | AAG | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(282): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.605+757_605+758del others(2): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713227 | |||||||
chr2:48713229 | G | C | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.605+757C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713229 | |||||||
chr2:48713231 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.605+755G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713231 | |||||||
chr2:48713449 | G | A | 5 | a0002c0002t0001g0209 a0002c0002t0001g0244 a0002c0002t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.605+537C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713449 | |||||||
chr2:48713476 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.605+510T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713476 | |||||||
chr2:48713478 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.605+508G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713478 | |||||||
chr2:48713490 | A | C | 20 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0172 others(17): Show |
20 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.605+496T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713490 | |||||||
chr2:48713494 | T | A | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(283): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.605+492A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713494 | |||||||
chr2:48713510 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.605+476T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713510 | |||||||
chr2:48713511 | G | A | 12 | a0001c0001t0001g0075 a0002c0002t0001g0016 a0002c0002t0001g0030 others(9): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.605+475C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713511 | |||||||
chr2:48713541 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.605+445G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713541 | |||||||
chr2:48713933 | CA | C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(69): Show |
74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.605+52delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713933 | |||||||
chr2:48713940 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0009g0217 |
2 | HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.605+46T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713940 | |||||||
chr2:48713948 | T | C | 1 | a0002c0002t0001g0315 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.605+38A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713948 | |||||||
chr2:48714163 | A | G | 2 | a0002c0002t0002g0310 a0003c0003t0002g0354 |
2 | HG01081.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.537-109T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714163 | |||||||
chr2:48714270 | A | T | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0318 |
3 | HG00423.hp1 HG02523.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.537-216T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714270 | |||||||
chr2:48714275 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.537-221G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714275 | |||||||
chr2:48714289 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.537-235G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714289 | |||||||
chr2:48714397 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.537-343G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714397 | |||||||
chr2:48714416 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.537-362C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714416 | |||||||
chr2:48714422 | G | A | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0318 |
3 | HG00423.hp1 HG02523.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.537-368C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714422 | |||||||
chr2:48714425 | T | C | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(95): Show |
103 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.537-371A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714425 | |||||||
chr2:48714483 | CTT | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-431_537-430del others(2): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714483 | |||||||
chr2:48714483 | CTTT | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0055 others(13): Show |
17 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.537-432_537-430del others(3): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714483 | |||||||
chr2:48714675 | A | G | 1 | a0002c0002t0003g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.537-621T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714675 | |||||||
chr2:48714740 | T | TAC | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(69): Show |
74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.537-688_537-687dup others(2): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714740 | |||||||
chr2:48714771 | G | A | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(283): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.537-717C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714771 | |||||||
chr2:48714897 | G | A | 1 | a0003c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.537-843C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714897 | |||||||
chr2:48714935 | T | G | 1 | a0002c0002t0003g0245 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.537-881A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714935 | |||||||
chr2:48715143 | T | A | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(283): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.537-1089A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715143 | |||||||
chr2:48715386 | G | A | 1 | a0002c0002t0004g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.537-1332C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715386 | |||||||
chr2:48715544 | G | T | 2 | a0002c0002t0003g0128 a0002c0002t0003g0208 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.537-1490C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715544 | |||||||
chr2:48715609 | T | A | 6 | a0002c0002t0001g0082 a0002c0002t0001g0229 a0003c0003t0001g0330 others(3): Show |
6 | HG01361.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.537-1555A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715609 | |||||||
chr2:48715623 | T | A | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.537-1569A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715623 | |||||||
chr2:48715868 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0004c0007t0003g0047 |
3 | HG00099.hp1 HG01123.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.537-1814G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715868 | |||||||
chr2:48716002 | G | T | 3 | a0002c0002t0001g0082 a0003c0003t0001g0330 a0003c0003t0001g0357 |
3 | HG01361.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.537-1948C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716002 | |||||||
chr2:48716056 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.537-2002C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716056 | |||||||
chr2:48716252 | G | C | 2 | a0001c0001t0001g0231 a0002c0002t0001g0315 |
2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.537-2198C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716252 | |||||||
chr2:48716657 | T | C | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.537-2603A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716657 | |||||||
chr2:48716661 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.537-2607G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716661 | |||||||
chr2:48716664 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(96): Show |
104 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.537-2610T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716664 | |||||||
chr2:48716701 | A | C | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.537-2647T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716701 | |||||||
chr2:48716948 | T | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0321 |
2 | HG00280.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.537-2894A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716948 | |||||||
chr2:48716948 | T | C | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.537-2894A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716948 | |||||||
chr2:48716951 | A | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.537-2897T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716951 | |||||||
chr2:48717035 | T | C | 1 | a0002c0002t0004g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.537-2981A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717035 | |||||||
chr2:48717048 | C | T | 3 | a0002c0002t0001g0234 a0002c0002t0004g0232 a0002c0002t0004g0294 |
3 | HG02622.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.537-2994G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717048 | |||||||
chr2:48717122 | C | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(96): Show |
104 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.537-3068G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717122 | |||||||
chr2:48717135 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3081C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717135 | |||||||
chr2:48717197 | A | G | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.537-3143T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717197 | |||||||
chr2:48717206 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.537-3152A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717206 | |||||||
chr2:48717302 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3248C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717302 | |||||||
chr2:48717303 | G | A | 1 | a0003c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.537-3249C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717303 | |||||||
chr2:48717394 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3340T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717394 | |||||||
chr2:48717407 | C | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3353G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717407 | |||||||
chr2:48717431 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(121): Show |
126 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.537-3377C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717431 | |||||||
chr2:48717474 | A | G | 1 | a0002c0002t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.537-3420T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717474 | |||||||
chr2:48717475 | A | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG01358.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.537-3421T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717475 | |||||||
chr2:48717486 | T | C | 1 | a0002c0002t0002g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.537-3432A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717486 | |||||||
chr2:48717542 | C | CTTA | 53 | a0001c0001t0001g0039 a0001c0001t0001g0075 a0001c0001t0001g0156 others(50): Show |
53 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.537-3491_537-3489d others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | |||||||
chr2:48717542 | C | CTTATTAT others(5): Show |
47 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(44): Show |
49 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.537-3500_537-3489d others(14): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | |||||||
chr2:48717542 | C | CTTATTAT others(8): Show |
13 | a0001c0001t0001g0101 a0001c0001t0001g0188 a0001c0001t0001g0207 others(10): Show |
13 | HG02080.hp1 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.537-3503_537-3489d others(17): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | |||||||
chr2:48717542 | C | CTTATTAT others(11): Show |
8 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0172 others(5): Show |
8 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.537-3506_537-3489d others(20): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | |||||||
chr2:48717542 | C | CTTATTAT others(14): Show |
2 | a0002c0002t0003g0170 a0002c0002t0003g0293 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.537-3489_537-3488i others(23): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | |||||||
chr2:48717542 | C | CTTATTAT others(20): Show |
1 | a0001c0001t0001g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.537-3489_537-3488i others(29): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | |||||||
chr2:48717605 | C | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(270): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.537-3551G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717605 | |||||||
chr2:48717833 | C | CT | 6 | a0001c0001t0001g0122 a0002c0002t0001g0234 a0002c0002t0002g0087 others(3): Show |
6 | HG02132.hp1 HG02622.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.537-3780dupA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717833 | |||||||
chr2:48717833 | CT | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(214): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.537-3780delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717833 | |||||||
chr2:48717833 | CTT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0063 others(46): Show |
52 | HG00099.hp2 HG01099.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.537-3781_537-3780d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717833 | |||||||
chr2:48717857 | C | T | 2 | a0002c0002t0004g0232 a0002c0002t0004g0294 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.537-3803G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717857 | |||||||
chr2:48717875 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3821C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717875 | |||||||
chr2:48718008 | C | T | 20 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0172 others(17): Show |
20 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.537-3954G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718008 | |||||||
chr2:48718073 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0130 |
2 | HG01261.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.537-4019T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718073 | |||||||
chr2:48718194 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-4140C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718194 | |||||||
chr2:48718346 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0071 others(37): Show |
43 | HG00099.hp2 HG01099.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.537-4292G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718346 | |||||||
chr2:48718611 | AT | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(67): Show |
72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.537-4558delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718611 | |||||||
chr2:48718633 | A | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.537-4579T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718633 | |||||||
chr2:48718703 | C | T | 1 | a0002c0002t0008g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.537-4649G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718703 | |||||||
chr2:48718735 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(67): Show |
72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.537-4681G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718735 | |||||||
chr2:48718765 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(67): Show |
72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.536+4691G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718765 | |||||||
chr2:48718815 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(67): Show |
72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.536+4641C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718815 | |||||||
chr2:48719028 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.536+4428T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719028 | |||||||
chr2:48719055 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.536+4401C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719055 | |||||||
chr2:48719061 | G | A | 2 | a0002c0002t0003g0128 a0002c0002t0003g0208 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.536+4395C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719061 | |||||||
chr2:48719091 | G | A | 1 | a0002c0002t0001g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.536+4365C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719091 | |||||||
chr2:48719093 | C | T | 2 | a0002c0002t0002g0273 a0002c0005t0002g0144 |
2 | NA18995.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.536+4363G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719093 | |||||||
chr2:48719094 | G | A | 33 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0028 others(30): Show |
34 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.536+4362C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719094 | |||||||
chr2:48719118 | C | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.536+4338G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719118 | |||||||
chr2:48719195 | G | A | 1 | a0003c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.536+4261C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719195 | |||||||
chr2:48719500 | C | G | 1 | a0003c0003t0003g0348 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.536+3956G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719500 | |||||||
chr2:48719564 | C | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | NA18960.hp2 NA19000.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.536+3892G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719564 | |||||||
chr2:48719579 | G | C | 1 | a0003c0003t0003g0348 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.536+3877C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719579 | |||||||
chr2:48719585 | T | C | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.536+3871A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719585 | |||||||
chr2:48719651 | T | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0002c0002t0001g0072 others(9): Show |
15 | HG01433.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.536+3805A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719651 | |||||||
chr2:48719741 | G | C | 4 | a0001c0001t0001g0129 a0002c0002t0001g0261 a0002c0002t0001g0284 others(1): Show |
4 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.536+3715C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719741 | |||||||
chr2:48719749 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.536+3707A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719749 | |||||||
chr2:48719767 | G | C | 1 | a0001c0006t0001g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.536+3689C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719767 | |||||||
chr2:48720063 | C | T | 3 | a0002c0002t0001g0234 a0002c0002t0004g0232 a0002c0002t0004g0294 |
3 | HG02622.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.536+3393G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720063 | |||||||
chr2:48720103 | C | A | 1 | a0002c0002t0002g0191 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.536+3353G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720103 | |||||||
chr2:48720197 | C | G | 1 | a0002c0002t0001g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.536+3259G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720197 | |||||||
chr2:48720207 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.536+3249T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720207 | |||||||
chr2:48720441 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(67): Show |
72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.536+3015C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720441 | |||||||
chr2:48720491 | A | T | 1 | a0002c0002t0002g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.536+2965T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720491 | |||||||
chr2:48720500 | T | C | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.536+2956A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720500 | |||||||
chr2:48720533 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.536+2923A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720533 | |||||||
chr2:48720611 | A | T | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.536+2845T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720611 | |||||||
chr2:48720863 | G | C | 1 | a0002c0002t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.536+2593C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720863 | |||||||
chr2:48720911 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0172 others(6): Show |
9 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.536+2545C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720911 | |||||||
chr2:48721055 | T | G | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.536+2401A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721055 | |||||||
chr2:48721196 | T | G | 1 | a0001c0012t0001g0023 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.536+2260A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721196 | |||||||
chr2:48721298 | C | G | 8 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0002g0237 others(5): Show |
8 | HG00099.hp2 HG01099.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.536+2158G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721298 | |||||||
chr2:48721568 | A | C | 87 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(84): Show |
91 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.536+1888T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721568 | |||||||
chr2:48721609 | C | T | 6 | a0002c0002t0003g0064 a0002c0002t0003g0128 a0002c0002t0003g0208 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.536+1847G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721609 | |||||||
chr2:48721663 | T | C | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.536+1793A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721663 | |||||||
chr2:48721717 | A | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.536+1739T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721717 | |||||||
chr2:48721742 | T | C | 1 | a0002c0002t0002g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.536+1714A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721742 | |||||||
chr2:48721839 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
11 | NA18944.hp1 NA18952.hp1 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.536+1617C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721839 | |||||||
chr2:48721929 | G | A | 4 | a0001c0001t0001g0178 a0001c0001t0001g0186 a0001c0001t0001g0282 others(1): Show |
4 | HG00673.hp1 HG02071.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+1527C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721929 | |||||||
chr2:48721997 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.536+1459T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721997 | |||||||
chr2:48722534 | T | G | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(98): Show |
106 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.536+922A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722534 | |||||||
chr2:48722539 | G | A | 1 | a0002c0002t0003g0245 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.536+917C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722539 | |||||||
chr2:48722788 | T | C | 5 | a0001c0001t0001g0233 a0002c0002t0003g0065 a0003c0003t0003g0329 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.536+668A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722788 | |||||||
chr2:48722893 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.536+563G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722893 | |||||||
chr2:48722902 | T | C | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.536+554A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722902 | |||||||
chr2:48722905 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0071 others(37): Show |
43 | HG00099.hp2 HG01099.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.536+551G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722905 | |||||||
chr2:48722936 | T | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0190 others(37): Show |
40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.536+520A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722936 | |||||||
chr2:48723099 | A | C | 1 | a0002c0002t0002g0222 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.536+357T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48723099 | |||||||
chr2:48723169 | AG | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
11 | NA18944.hp1 NA18952.hp1 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.536+286delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48723169 | |||||||
chr2:48723263 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.536+193C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48723263 | |||||||
chr2:48723316 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.536+140G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48723316 | |||||||
chr2:48724056 | C | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | NA18960.hp2 NA19000.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-360G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724056 | |||||||
chr2:48724352 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.384-656C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724352 | |||||||
chr2:48724816 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0003c0004t0001g0333 others(1): Show |
4 | HG00639.hp2 HG01109.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+860A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724816 | |||||||
chr2:48724832 | G | C | 96 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(93): Show |
101 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.383+844C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724832 | |||||||
chr2:48724870 | G | A | 1 | a0002c0002t0002g0311 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.383+806C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724870 | |||||||
chr2:48724934 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.383+742C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724934 | |||||||
chr2:48725064 | A | G | 1 | a0002c0002t0002g0322 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.383+612T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725064 | |||||||
chr2:48725310 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.383+366T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725310 | |||||||
chr2:48725350 | A | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG02886.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.383+326T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725350 | |||||||
chr2:48725355 | C | A | 1 | a0002c0002t0002g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.383+321G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725355 | |||||||
chr2:48725435 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.383+241G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725435 | |||||||
chr2:48725485 | G | A | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(355): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.383+191C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725485 | |||||||
chr2:48725499 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.383+177G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725499 | |||||||
chr2:48725510 | G | A | 46 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0154 others(43): Show |
46 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.383+166C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725510 | |||||||
chr2:48725562 | C | G | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(355): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.383+114G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725562 | |||||||
chr2:48725805 | A | G | 3 | a0002c0002t0001g0234 a0002c0002t0004g0232 a0002c0002t0004g0294 |
3 | HG02622.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.309-55T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48725805 | |||||||
chr2:48725886 | G | A | 1 | a0002c0005t0002g0144 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.309-136C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48725886 | |||||||
chr2:48726070 | C | T | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(349): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.309-320G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726070 | |||||||
chr2:48726117 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0089 others(76): Show |
83 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.309-367G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726117 | |||||||
chr2:48726210 | C | T | 186 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.309-460G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726210 | |||||||
chr2:48726390 | G | C | 1 | a0001c0001t0001g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.309-640C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726390 | |||||||
chr2:48726421 | G | A | 2 | a0002c0002t0005g0250 a0002c0002t0005g0326 |
2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.309-671C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726421 | |||||||
chr2:48726495 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.309-745C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726495 | |||||||
chr2:48726601 | G | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0102 others(44): Show |
49 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.309-851C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726601 | |||||||
chr2:48726626 | C | T | 2 | a0002c0002t0001g0297 a0004c0007t0003g0296 |
2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.309-876G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726626 | |||||||
chr2:48726730 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.309-980C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726730 | |||||||
chr2:48726808 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0102 others(25): Show |
29 | HG00280.hp1 HG00558.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.309-1058C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726808 | |||||||
chr2:48726840 | T | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(109): Show |
114 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.309-1090A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726840 | |||||||
chr2:48727031 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.309-1281A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727031 | |||||||
chr2:48727142 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.309-1392A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727142 | |||||||
chr2:48727230 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-1480C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727230 | |||||||
chr2:48727288 | A | C | 2 | a0001c0001t0001g0264 a0002c0002t0001g0246 |
2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.309-1538T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727288 | |||||||
chr2:48727289 | A | T | 2 | a0001c0001t0001g0264 a0002c0002t0001g0246 |
2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.309-1539T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727289 | |||||||
chr2:48727461 | A | G | 1 | a0003c0003t0002g0340 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.308+1692T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727461 | |||||||
chr2:48727644 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.308+1509A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727644 | |||||||
chr2:48727703 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.308+1450T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727703 | |||||||
chr2:48727766 | T | C | 106 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(103): Show |
107 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.308+1387A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727766 | |||||||
chr2:48727890 | T | C | 1 | a0002c0002t0003g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.308+1263A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727890 | |||||||
chr2:48727901 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.308+1252T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727901 | |||||||
chr2:48727942 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.308+1211T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727942 | |||||||
chr2:48728046 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.308+1107G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728046 | |||||||
chr2:48728083 | A | G | 2 | a0002c0002t0001g0070 a0002c0002t0001g0079 |
2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.308+1070T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728083 | |||||||
chr2:48728087 | GT | G | 105 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0094 others(102): Show |
106 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.308+1065delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728087 | |||||||
chr2:48728087 | GTT | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
111 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.308+1064_308+1065d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728087 | |||||||
chr2:48728087 | GTTT | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.308+1063_308+1065d others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728087 | |||||||
chr2:48728175 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.308+978A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728175 | |||||||
chr2:48728198 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.308+955G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728198 | |||||||
chr2:48728231 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.308+922G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728231 | |||||||
chr2:48728266 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.308+887G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728266 | |||||||
chr2:48728348 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.308+805A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728348 | |||||||
chr2:48728362 | A | G | 1 | a0005c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.308+791T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728362 | |||||||
chr2:48728422 | C | G | 1 | a0001c0001t0001g0277 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.308+731G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728422 | |||||||
chr2:48728510 | C | G | 1 | a0001c0001t0006g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.308+643G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728510 | |||||||
chr2:48728531 | T | C | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.308+622A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728531 | |||||||
chr2:48728544 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.308+609T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728544 | |||||||
chr2:48728590 | T | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | HG00438.hp1 HG02027.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.308+563A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728590 | |||||||
chr2:48729278 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.234-51G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729278 | |||||||
chr2:48729292 | T | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.234-65A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729292 | |||||||
chr2:48729332 | G | C | 1 | a0004c0007t0003g0316 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.234-105C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729332 | |||||||
chr2:48729336 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.234-109G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729336 | |||||||
chr2:48729373 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.234-146T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729373 | |||||||
chr2:48729373 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.234-146T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729373 | |||||||
chr2:48729659 | A | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02040.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.234-432T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729659 | |||||||
chr2:48729773 | T | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02015.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.234-546A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729773 | |||||||
chr2:48729844 | T | C | 1 | a0002c0002t0002g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.234-617A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729844 | |||||||
chr2:48729972 | AC | A | 2 | a0003c0008t0004g0012 a0003c0008t0004g0361 |
3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.234-746delG | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729972 | |||||||
chr2:48730016 | A | G | 1 | a0005c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234-789T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48730016 | |||||||
chr2:48730206 | G | A | 1 | a0005c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234-979C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48730206 | |||||||
chr2:48730442 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
67 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.233+785T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48730442 | |||||||
chr2:48730720 | C | T | 1 | a0003c0004t0001g0336 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.233+507G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48730720 | |||||||
chr2:48731132 | C | T | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.233+95G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48731132 | |||||||
chr2:48731152 | T | A | 9 | a0002c0002t0001g0016 a0002c0002t0001g0030 a0002c0002t0001g0037 others(6): Show |
10 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+75A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48731152 | |||||||
chr2:48731456 | A | G | 33 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(30): Show |
34 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.162-158T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731456 | |||||||
chr2:48731487 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
112 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.162-189T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731487 | |||||||
chr2:48731508 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
112 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.162-210G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731508 | |||||||
chr2:48731548 | G | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
112 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.162-250C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731548 | |||||||
chr2:48731608 | C | T | 2 | a0003c0003t0002g0340 a0003c0003t0002g0355 |
2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.162-310G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731608 | |||||||
chr2:48731889 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02040.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.162-591G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731889 | |||||||
chr2:48732135 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.162-837C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732135 | |||||||
chr2:48732166 | G | T | 1 | a0001c0001t0001g0303 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.162-868C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732166 | |||||||
chr2:48732280 | G | A | 1 | a0004c0007t0003g0296 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.162-982C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732280 | |||||||
chr2:48732312 | G | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(28): Show |
32 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-1014C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732312 | |||||||
chr2:48732398 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
115 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.162-1100A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732398 | |||||||
chr2:48732405 | C | T | 2 | a0003c0008t0004g0012 a0003c0008t0004g0361 |
3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.162-1107G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732405 | |||||||
chr2:48732464 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.162-1166T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732464 | |||||||
chr2:48732582 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.162-1284G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732582 | |||||||
chr2:48732628 | C | T | 3 | a0002c0002t0004g0068 a0003c0003t0004g0334 a0003c0003t0004g0338 |
3 | HG02559.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.162-1330G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732628 | |||||||
chr2:48732734 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.162-1436G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732734 | |||||||
chr2:48732766 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.162-1468C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732766 | |||||||
chr2:48732824 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.162-1526T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732824 | |||||||
chr2:48732864 | A | G | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.162-1566T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732864 | |||||||
chr2:48732893 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(49): Show |
55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.162-1595C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732893 | |||||||
chr2:48732973 | A | G | 8 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0299 others(5): Show |
8 | HG00423.hp1 HG02523.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-1675T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732973 | |||||||
chr2:48733173 | T | G | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-1875A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733173 | |||||||
chr2:48733178 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
157 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.162-1880T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733178 | |||||||
chr2:48733194 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-1896G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733194 | |||||||
chr2:48733372 | G | A | 1 | a0001c0001t0006g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.162-2074C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733372 | |||||||
chr2:48733380 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.162-2082A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733380 | |||||||
chr2:48733501 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(49): Show |
55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.162-2203G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733501 | |||||||
chr2:48733671 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(49): Show |
55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.162-2373C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733671 | |||||||
chr2:48733765 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.162-2467A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733765 | |||||||
chr2:48733804 | G | A | 6 | a0001c0001t0001g0233 a0002c0002t0001g0234 a0002c0002t0001g0297 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-2506C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733804 | |||||||
chr2:48733804 | G | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-2506C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733804 | |||||||
chr2:48733936 | A | G | 1 | a0003c0003t0002g0340 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.162-2638T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733936 | |||||||
chr2:48734017 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.162-2719A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734017 | |||||||
chr2:48734108 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162-2810C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734108 | |||||||
chr2:48734147 | C | A | 2 | a0003c0008t0004g0012 a0003c0008t0004g0361 |
3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.162-2849G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734147 | |||||||
chr2:48734199 | A | T | 32 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(29): Show |
33 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-2901T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734199 | |||||||
chr2:48734256 | C | T | 3 | a0002c0002t0004g0068 a0003c0003t0004g0334 a0003c0003t0004g0338 |
3 | HG02559.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.162-2958G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734256 | |||||||
chr2:48734257 | G | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(49): Show |
55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.162-2959C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734257 | |||||||
chr2:48734312 | A | G | 1 | a0002c0002t0001g0243 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162-3014T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734312 | |||||||
chr2:48734418 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.162-3120C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734418 | |||||||
chr2:48734502 | A | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
112 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.162-3204T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734502 | |||||||
chr2:48734523 | A | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
56 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.162-3225T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734523 | |||||||
chr2:48734563 | TTCC | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.162-3268_162-3266d others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734563 | |||||||
chr2:48734811 | G | T | 3 | a0002c0002t0001g0016 a0002c0002t0001g0030 a0002c0002t0001g0037 |
3 | HG02055.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.162-3513C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734811 | |||||||
chr2:48734858 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(51): Show |
57 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.162-3560T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734858 | |||||||
chr2:48734884 | T | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0061 |
3 | HG02273.hp1 NA19003.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.162-3586A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734884 | |||||||
chr2:48734888 | G | A | 2 | a0002c0002t0003g0170 a0002c0002t0005g0081 |
2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.162-3590C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734888 | |||||||
chr2:48734978 | A | G | 1 | a0002c0002t0003g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162-3680T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734978 | |||||||
chr2:48735152 | G | T | 38 | a0001c0001t0001g0233 a0001c0001t0001g0287 a0002c0002t0001g0234 others(35): Show |
38 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.162-3854C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735152 | |||||||
chr2:48735216 | T | A | 4 | a0002c0002t0001g0016 a0002c0002t0001g0030 a0002c0002t0001g0037 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-3918A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735216 | |||||||
chr2:48735271 | T | C | 1 | a0003c0008t0004g0361 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162-3973A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735271 | |||||||
chr2:48735296 | A | T | 1 | a0003c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.162-3998T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735296 | |||||||
chr2:48735304 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.162-4006C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735304 | |||||||
chr2:48735411 | A | G | 3 | a0002c0002t0004g0068 a0003c0003t0004g0334 a0003c0003t0004g0338 |
3 | HG02559.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.162-4113T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735411 | |||||||
chr2:48735485 | T | C | 12 | a0003c0003t0002g0354 a0003c0003t0003g0329 a0003c0003t0003g0331 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.162-4187A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735485 | |||||||
chr2:48735633 | C | T | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.162-4335G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735633 | |||||||
chr2:48735674 | G | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
56 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.162-4376C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735674 | |||||||
chr2:48735743 | G | A | 5 | a0001c0001t0001g0136 a0002c0002t0002g0009 a0002c0002t0002g0083 others(2): Show |
6 | HG00642.hp1 HG00738.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-4445C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735743 | |||||||
chr2:48735763 | G | A | 2 | a0001c0001t0001g0264 a0002c0002t0001g0246 |
2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.162-4465C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735763 | |||||||
chr2:48735786 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0134 a0001c0001t0001g0135 others(5): Show |
9 | NA18944.hp1 NA18952.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-4488C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735786 | |||||||
chr2:48735815 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.162-4517A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735815 | |||||||
chr2:48735921 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0173 others(6): Show |
9 | HG00438.hp2 HG02523.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-4623G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735921 | |||||||
chr2:48736146 | A | G | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-4848T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736146 | |||||||
chr2:48736405 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.162-5107G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736405 | |||||||
chr2:48736490 | C | T | 2 | a0002c0002t0001g0297 a0004c0007t0003g0296 |
2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.162-5192G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736490 | |||||||
chr2:48736730 | A | G | 1 | a0003c0004t0001g0359 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.162-5432T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736730 | |||||||
chr2:48736854 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.162-5556A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736854 | |||||||
chr2:48736891 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.162-5593A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736891 | |||||||
chr2:48737045 | G | A | 47 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0075 others(44): Show |
49 | HG00280.hp2 HG00733.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.162-5747C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737045 | |||||||
chr2:48737068 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-5770C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737068 | |||||||
chr2:48737242 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-5944T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737242 | |||||||
chr2:48737281 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.162-5983A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737281 | |||||||
chr2:48737318 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162-6020C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737318 | |||||||
chr2:48737427 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162-6129T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737427 | |||||||
chr2:48737438 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.162-6140A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737438 | |||||||
chr2:48737571 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
204 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.162-6273A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737571 | |||||||
chr2:48737588 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0002c0002t0002g0109 |
3 | HG02572.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.162-6290G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737588 | |||||||
chr2:48737589 | G | A | 3 | a0002c0002t0001g0244 a0002c0002t0003g0014 a0002c0002t0003g0245 |
3 | HG02486.hp1 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162-6291C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737589 | |||||||
chr2:48737613 | G | A | 2 | a0001c0001t0001g0292 a0002c0002t0003g0293 |
2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.162-6315C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737613 | |||||||
chr2:48737753 | C | A | 1 | a0001c0001t0006g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.162-6455G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737753 | |||||||
chr2:48737846 | A | T | 1 | a0003c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.162-6548T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737846 | |||||||
chr2:48737860 | C | G | 1 | a0001c0001t0001g0230 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.162-6562G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737860 | |||||||
chr2:48737883 | A | C | 33 | a0001c0001t0001g0287 a0002c0002t0004g0068 a0002c0002t0008g0098 others(30): Show |
33 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-6585T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737883 | |||||||
chr2:48738093 | A | G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0172 a0001c0001t0001g0218 others(1): Show |
4 | HG00140.hp1 HG01515.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-6795T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738093 | |||||||
chr2:48738189 | C | A | 1 | a0002c0002t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162-6891G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738189 | |||||||
chr2:48738464 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
128 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.162-7166A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738464 | |||||||
chr2:48738569 | C | T | 1 | a0003c0003t0003g0348 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162-7271G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738569 | |||||||
chr2:48738643 | G | A | 1 | a0002c0002t0002g0169 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.162-7345C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738643 | |||||||
chr2:48738707 | T | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
128 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.162-7409A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738707 | |||||||
chr2:48738739 | A | G | 30 | a0001c0001t0001g0010 a0001c0001t0001g0086 a0001c0001t0001g0122 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.162-7441T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738739 | |||||||
chr2:48738842 | T | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
205 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.162-7544A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738842 | |||||||
chr2:48738846 | T | C | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.162-7548A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738846 | |||||||
chr2:48738900 | A | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.162-7602T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738900 | |||||||
chr2:48738916 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
190 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.162-7618G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738916 | |||||||
chr2:48738999 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.162-7701A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738999 | |||||||
chr2:48739007 | T | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-7709A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739007 | |||||||
chr2:48739021 | C | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.162-7723G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739021 | |||||||
chr2:48739200 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0327 |
2 | HG01361.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.162-7902A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739200 | |||||||
chr2:48739215 | G | C | 2 | a0001c0001t0001g0125 a0001c0001t0006g0126 |
2 | NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.162-7917C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739215 | |||||||
chr2:48739255 | G | A | 6 | a0003c0003t0001g0330 a0003c0003t0001g0353 a0003c0003t0001g0357 others(3): Show |
6 | HG01257.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-7957C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739255 | |||||||
chr2:48739288 | T | C | 1 | a0002c0002t0003g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162-7990A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739288 | |||||||
chr2:48739375 | C | T | 2 | a0001c0001t0001g0075 a0005c0009t0004g0069 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.162-8077G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739375 | |||||||
chr2:48739379 | A | G | 10 | a0001c0001t0001g0287 a0003c0003t0002g0346 a0003c0003t0002g0347 others(7): Show |
10 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-8081T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739379 | |||||||
chr2:48739501 | TG | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
12 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.162-8204delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739501 | |||||||
chr2:48739518 | T | C | 3 | a0001c0001t0001g0129 a0002c0002t0001g0244 a0002c0002t0003g0245 |
3 | HG02451.hp2 HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162-8220A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739518 | |||||||
chr2:48739604 | T | C | 4 | a0002c0002t0005g0250 a0002c0002t0005g0326 a0003c0008t0004g0012 others(1): Show |
5 | HG02630.hp1 HG02896.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-8306A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739604 | |||||||
chr2:48739637 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.162-8339C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739637 | |||||||
chr2:48739668 | G | C | 9 | a0001c0001t0001g0287 a0003c0003t0002g0346 a0003c0003t0002g0347 others(6): Show |
9 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-8370C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739668 | |||||||
chr2:48739746 | G | C | 2 | a0002c0002t0003g0110 a0002c0002t0003g0112 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.162-8448C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739746 | |||||||
chr2:48739814 | A | T | 10 | a0001c0001t0001g0207 a0001c0001t0001g0265 a0001c0001t0001g0266 others(7): Show |
10 | HG01109.hp1 HG01358.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-8516T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739814 | |||||||
chr2:48739863 | C | G | 1 | a0002c0002t0002g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.162-8565G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739863 | |||||||
chr2:48739882 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.162-8584C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739882 | |||||||
chr2:48739992 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.162-8694G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739992 | |||||||
chr2:48739993 | G | A | 5 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0301 others(2): Show |
5 | NA18945.hp2 NA18950.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-8695C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739993 | |||||||
chr2:48740004 | C | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-8706G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740004 | |||||||
chr2:48740035 | C | T | 1 | a0002c0002t0002g0200 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.162-8737G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740035 | |||||||
chr2:48740128 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.162-8830A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740128 | |||||||
chr2:48740181 | G | A | 2 | a0002c0002t0001g0244 a0002c0002t0003g0245 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162-8883C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740181 | |||||||
chr2:48740246 | G | T | 2 | a0003c0004t0001g0332 a0003c0004t0001g0351 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.162-8948C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740246 | |||||||
chr2:48740334 | C | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
62 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.162-9036G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740334 | |||||||
chr2:48740416 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.162-9118A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740416 | |||||||
chr2:48740441 | T | G | 2 | a0003c0003t0003g0343 a0003c0004t0001g0344 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.162-9143A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740441 | |||||||
chr2:48740462 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0006t0001g0225 others(1): Show |
4 | HG00741.hp2 HG01361.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-9164C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740462 | |||||||
chr2:48740543 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.162-9245A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740543 | |||||||
chr2:48740544 | G | A | 4 | a0001c0001t0001g0111 a0002c0002t0003g0110 a0002c0002t0003g0112 others(1): Show |
4 | HG01243.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-9246C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740544 | |||||||
chr2:48740557 | G | A | 4 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0301 others(1): Show |
4 | NA18950.hp2 NA18974.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-9259C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740557 | |||||||
chr2:48740566 | C | G | 15 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0002c0002t0001g0070 others(12): Show |
16 | HG01891.hp2 HG02145.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.162-9268G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740566 | |||||||
chr2:48740596 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.162-9298A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740596 | |||||||
chr2:48740600 | C | A | 2 | a0001c0001t0001g0207 a0002c0002t0003g0262 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162-9302G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740600 | |||||||
chr2:48740606 | C | T | 2 | a0001c0001t0001g0207 a0002c0002t0003g0262 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162-9308G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740606 | |||||||
chr2:48740619 | G | A | 1 | a0002c0002t0002g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.162-9321C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740619 | |||||||
chr2:48740770 | A | T | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9472T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740770 | |||||||
chr2:48740782 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9484A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740782 | |||||||
chr2:48740783 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9485C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740783 | |||||||
chr2:48740789 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9491G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740789 | |||||||
chr2:48740811 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9513A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740811 | |||||||
chr2:48740845 | G | T | 2 | a0003c0003t0002g0340 a0003c0003t0002g0355 |
2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.162-9547C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740845 | |||||||
chr2:48740899 | C | G | 1 | a0003c0004t0001g0337 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.162-9601G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740899 | |||||||
chr2:48741067 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.162-9769C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741067 | |||||||
chr2:48741085 | G | A | 1 | a0002c0002t0003g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162-9787C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741085 | |||||||
chr2:48741121 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.162-9823A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741121 | |||||||
chr2:48741235 | G | A | 5 | a0002c0002t0001g0209 a0002c0002t0004g0189 a0002c0002t0004g0210 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-9937C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741235 | |||||||
chr2:48741362 | G | A | 1 | a0001c0006t0001g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.162-10064C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741362 | |||||||
chr2:48741427 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-10129T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741427 | |||||||
chr2:48741453 | T | TA | 72 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(69): Show |
74 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-10156dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741453 | |||||||
chr2:48741464 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-10166C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741464 | |||||||
chr2:48741538 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
258 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.162-10240G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741538 | |||||||
chr2:48741592 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-10294T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741592 | |||||||
chr2:48741662 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162-10364C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741662 | |||||||
chr2:48741691 | G | A | 25 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0299 others(22): Show |
25 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.162-10393C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741691 | |||||||
chr2:48741787 | G | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-10489C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741787 | |||||||
chr2:48741949 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.162-10651C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741949 | |||||||
chr2:48741953 | C | T | 2 | a0003c0008t0004g0012 a0003c0008t0004g0361 |
3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.162-10655G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741953 | |||||||
chr2:48742026 | G | A | 57 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0090 others(54): Show |
57 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.162-10728C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742026 | |||||||
chr2:48742050 | T | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.162-10752A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742050 | |||||||
chr2:48742093 | A | G | 37 | a0001c0001t0001g0287 a0002c0002t0003g0097 a0002c0002t0004g0068 others(34): Show |
37 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.162-10795T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742093 | |||||||
chr2:48742118 | G | A | 1 | a0002c0002t0001g0270 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.162-10820C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742118 | |||||||
chr2:48742184 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162-10886A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742184 | |||||||
chr2:48742330 | C | T | 1 | a0005c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-11032G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742330 | |||||||
chr2:48742452 | C | T | 2 | a0001c0001t0001g0319 a0002c0002t0001g0325 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.162-11154G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742452 | |||||||
chr2:48742497 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-11199T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742497 | |||||||
chr2:48742550 | G | A | 1 | a0005c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-11252C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742550 | |||||||
chr2:48742605 | C | T | 1 | a0002c0002t0005g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162-11307G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742605 | |||||||
chr2:48742606 | A | G | 1 | a0002c0002t0005g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162-11308T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742606 | |||||||
chr2:48742622 | T | G | 4 | a0001c0001t0001g0287 a0003c0003t0002g0346 a0003c0003t0002g0347 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-11324A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742622 | |||||||
chr2:48742645 | G | A | 1 | a0002c0002t0002g0281 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.162-11347C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742645 | |||||||
chr2:48742681 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0040 |
2 | HG02273.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.162-11383C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742681 | |||||||
chr2:48742711 | T | A | 1 | a0002c0002t0001g0243 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162-11413A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742711 | |||||||
chr2:48742769 | C | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.162-11471G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742769 | |||||||
chr2:48742923 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.162-11625G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742923 | |||||||
chr2:48742971 | G | T | 3 | a0002c0002t0003g0014 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02630.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162-11673C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742971 | |||||||
chr2:48743006 | G | A | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.162-11708C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743006 | |||||||
chr2:48743020 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.162-11722C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743020 | |||||||
chr2:48743070 | T | A | 1 | a0005c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-11772A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743070 | |||||||
chr2:48743100 | G | T | 1 | a0001c0001t0001g0298 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.162-11802C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743100 | |||||||
chr2:48743145 | A | G | 2 | a0002c0002t0001g0244 a0002c0002t0003g0245 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162-11847T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743145 | |||||||
chr2:48743180 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.162-11882G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743180 | |||||||
chr2:48743203 | A | G | 1 | a0003c0004t0001g0359 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.162-11905T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743203 | |||||||
chr2:48743247 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.162-11949G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743247 | |||||||
chr2:48743296 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.162-11998G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743296 | |||||||
chr2:48743319 | G | C | 1 | a0002c0002t0005g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.162-12021C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743319 | |||||||
chr2:48743326 | C | A | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-12028G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743326 | |||||||
chr2:48743346 | G | A | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-12048C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743346 | |||||||
chr2:48743430 | T | A | 1 | a0002c0002t0002g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.161+12081A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743430 | |||||||
chr2:48743431 | A | G | 1 | a0002c0002t0002g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.161+12080T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743431 | |||||||
chr2:48743451 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.161+12060C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743451 | |||||||
chr2:48743645 | C | A | 3 | a0001c0001t0001g0156 a0002c0002t0002g0155 a0002c0002t0002g0157 |
3 | NA18948.hp1 NA18951.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.161+11866G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743645 | |||||||
chr2:48743650 | A | T | 1 | a0002c0002t0008g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.161+11861T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743650 | |||||||
chr2:48743748 | G | A | 4 | a0001c0001t0001g0314 a0002c0002t0001g0315 a0002c0002t0002g0313 others(1): Show |
4 | HG00280.hp1 HG02486.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+11763C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743748 | |||||||
chr2:48743891 | A | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02015.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.161+11620T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743891 | |||||||
chr2:48743957 | G | C | 1 | a0001c0001t0001g0259 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.161+11554C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743957 | |||||||
chr2:48744003 | A | G | 1 | a0002c0002t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.161+11508T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744003 | |||||||
chr2:48744015 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
231 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.161+11496G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744015 | |||||||
chr2:48744107 | G | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.161+11404C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744107 | |||||||
chr2:48744114 | A | G | 3 | a0002c0002t0001g0295 a0002c0002t0001g0297 a0004c0007t0003g0296 |
3 | HG02451.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.161+11397T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744114 | |||||||
chr2:48744183 | G | T | 20 | a0001c0001t0001g0207 a0001c0001t0001g0263 a0001c0001t0001g0264 others(17): Show |
20 | HG01109.hp1 HG01358.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.161+11328C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744183 | |||||||
chr2:48744229 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.161+11282A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744229 | |||||||
chr2:48744266 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.161+11245A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744266 | |||||||
chr2:48744304 | A | G | 1 | a0002c0002t0008g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.161+11207T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744304 | |||||||
chr2:48744343 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.161+11168T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744343 | |||||||
chr2:48744376 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161+11135A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744376 | |||||||
chr2:48744417 | A | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+11094T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744417 | |||||||
chr2:48744431 | C | G | 2 | a0002c0002t0004g0080 a0002c0002t0005g0067 |
2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.161+11080G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744431 | |||||||
chr2:48744505 | C | T | 3 | a0002c0002t0001g0016 a0002c0002t0001g0030 a0002c0002t0001g0037 |
3 | HG02055.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.161+11006G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744505 | |||||||
chr2:48744540 | G | A | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+10971C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744540 | |||||||
chr2:48744643 | T | C | 1 | a0002c0002t0001g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161+10868A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744643 | |||||||
chr2:48744755 | C | T | 2 | a0002c0002t0001g0244 a0002c0002t0003g0245 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.161+10756G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744755 | |||||||
chr2:48744835 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.161+10676T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744835 | |||||||
chr2:48744853 | A | G | 3 | a0001c0001t0001g0111 a0002c0002t0003g0110 a0002c0002t0003g0112 |
3 | HG01243.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.161+10658T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744853 | |||||||
chr2:48744899 | G | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+10612C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744899 | |||||||
chr2:48744932 | T | C | 3 | a0002c0002t0001g0295 a0002c0002t0001g0297 a0004c0007t0003g0296 |
3 | HG02451.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.161+10579A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744932 | |||||||
chr2:48744935 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.161+10576G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744935 | |||||||
chr2:48744968 | C | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
6 | NA18952.hp1 NA19010.hp1 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+10543G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744968 | |||||||
chr2:48745032 | G | A | 2 | a0003c0004t0001g0332 a0003c0004t0001g0351 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.161+10479C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745032 | |||||||
chr2:48745070 | A | G | 2 | a0001c0001t0001g0036 a0001c0006t0001g0260 |
2 | HG00099.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.161+10441T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745070 | |||||||
chr2:48745166 | G | T | 6 | a0001c0001t0001g0094 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | NA18968.hp2 NA18983.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+10345C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745166 | |||||||
chr2:48745401 | G | A | 1 | a0005c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161+10110C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745401 | |||||||
chr2:48745413 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(150): Show |
161 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(158): Show |
intron_variant | MODIFIER | c.161+10098T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745413 | |||||||
chr2:48745458 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.161+10053T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745458 | |||||||
chr2:48745525 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.161+9986T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745525 | |||||||
chr2:48745535 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
125 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.161+9976G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745535 | |||||||
chr2:48745880 | GA | G | 10 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
12 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.161+9630delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745880 | |||||||
chr2:48745881 | A | G | 30 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0299 others(27): Show |
30 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.161+9630T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745881 | |||||||
chr2:48745882 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
10 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.161+9629T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745882 | |||||||
chr2:48745914 | T | C | 1 | a0003c0004t0001g0356 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.161+9597A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745914 | |||||||
chr2:48745949 | C | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.161+9562G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745949 | |||||||
chr2:48745988 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
126 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.161+9523C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745988 | |||||||
chr2:48745991 | C | G | 3 | a0002c0002t0003g0014 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02630.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161+9520G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745991 | |||||||
chr2:48746023 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.161+9488A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746023 | |||||||
chr2:48746056 | A | G | 27 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0299 others(24): Show |
27 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.161+9455T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746056 | |||||||
chr2:48746213 | G | A | 3 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0283 |
3 | HG02723.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.161+9298C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746213 | |||||||
chr2:48746221 | G | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.161+9290C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746221 | |||||||
chr2:48746252 | G | C | 2 | a0002c0002t0001g0229 a0002c0002t0002g0150 |
2 | HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.161+9259C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746252 | |||||||
chr2:48746278 | A | G | 1 | a0005c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161+9233T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746278 | |||||||
chr2:48746296 | A | C | 4 | a0001c0001t0001g0233 a0002c0002t0001g0234 a0002c0002t0004g0232 others(1): Show |
4 | HG02572.hp1 HG02622.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+9215T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746296 | |||||||
chr2:48746889 | T | G | 2 | a0002c0002t0001g0139 a0002c0002t0001g0204 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161+8622A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746889 | |||||||
chr2:48746990 | CCT | C | 26 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0299 others(23): Show |
26 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.161+8519_161+8520d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746990 | |||||||
chr2:48747091 | C | CT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0062 a0001c0001t0001g0089 others(18): Show |
23 | HG01099.hp1 HG01106.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.161+8419dupA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747091 | |||||||
chr2:48747091 | C | CTT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.161+8418_161+8419d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747091 | |||||||
chr2:48747131 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.161+8380T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747131 | |||||||
chr2:48747264 | T | C | 2 | a0003c0003t0003g0343 a0003c0004t0001g0344 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.161+8247A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747264 | |||||||
chr2:48747358 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.161+8153G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747358 | |||||||
chr2:48747495 | G | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.161+8016C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747495 | |||||||
chr2:48747510 | T | A | 27 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0299 others(24): Show |
27 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.161+8001A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747510 | |||||||
chr2:48747600 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161+7911G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747600 | |||||||
chr2:48747611 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02027.hp2 HG02132.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+7900A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747611 | |||||||
chr2:48747728 | T | G | 1 | a0001c0006t0001g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.161+7783A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747728 | |||||||
chr2:48747758 | C | G | 9 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0299 others(6): Show |
9 | HG00423.hp1 HG02523.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.161+7753G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747758 | |||||||
chr2:48747830 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.161+7681G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747830 | |||||||
chr2:48747843 | C | T | 2 | a0002c0002t0001g0244 a0002c0002t0003g0245 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.161+7668G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747843 | |||||||
chr2:48748159 | C | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
86 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.161+7352G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748159 | |||||||
chr2:48748353 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.161+7158C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748353 | |||||||
chr2:48748407 | C | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.161+7104G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748407 | |||||||
chr2:48748492 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.161+7019C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748492 | |||||||
chr2:48748667 | T | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0002c0002t0002g0109 |
3 | HG02572.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.161+6844A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748667 | |||||||
chr2:48748689 | T | C | 2 | a0002c0002t0003g0110 a0002c0002t0003g0112 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6822A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748689 | |||||||
chr2:48748693 | T | G | 2 | a0002c0002t0003g0110 a0002c0002t0003g0112 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6818A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748693 | |||||||
chr2:48748694 | A | T | 2 | a0002c0002t0003g0110 a0002c0002t0003g0112 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6817T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748694 | |||||||
chr2:48748695 | C | G | 2 | a0002c0002t0003g0110 a0002c0002t0003g0112 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6816G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748695 | |||||||
chr2:48748700 | A | G | 2 | a0002c0002t0003g0110 a0002c0002t0003g0112 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6811T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748700 | |||||||
chr2:48748701 | T | A | 2 | a0002c0002t0003g0110 a0002c0002t0003g0112 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6810A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748701 | |||||||
chr2:48748703 | C | G | 2 | a0002c0002t0003g0110 a0002c0002t0003g0112 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6808G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748703 | |||||||
chr2:48748856 | C | T | 2 | a0002c0002t0001g0244 a0002c0002t0003g0245 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.161+6655G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748856 | |||||||
chr2:48748970 | C | T | 3 | a0001c0001t0001g0156 a0002c0002t0002g0155 a0002c0002t0002g0157 |
3 | NA18948.hp1 NA18951.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.161+6541G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748970 | |||||||
chr2:48749071 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.161+6440C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749071 | |||||||
chr2:48749088 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.161+6423T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749088 | |||||||
chr2:48749088 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.161+6423T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749088 | |||||||
chr2:48749093 | A | C | 2 | a0003c0003t0003g0343 a0003c0004t0001g0344 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.161+6418T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749093 | |||||||
chr2:48749167 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0035 |
4 | HG00621.hp2 HG01109.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+6344G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749167 | |||||||
chr2:48749200 | A | G | 2 | a0003c0008t0004g0012 a0003c0008t0004g0361 |
3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.161+6311T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749200 | |||||||
chr2:48749209 | C | T | 2 | a0002c0002t0005g0250 a0002c0002t0005g0326 |
2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.161+6302G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749209 | |||||||
chr2:48749259 | G | A | 1 | a0003c0004t0001g0336 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.161+6252C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749259 | |||||||
chr2:48749276 | G | A | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+6235C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749276 | |||||||
chr2:48749314 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.161+6197A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749314 | |||||||
chr2:48749438 | C | G | 16 | a0003c0003t0001g0330 a0003c0003t0001g0353 a0003c0003t0001g0357 others(13): Show |
16 | HG00639.hp2 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.161+6073G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749438 | |||||||
chr2:48749493 | A | G | 3 | a0002c0002t0003g0014 a0002c0002t0005g0250 a0002c0002t0005g0326 |
3 | HG02630.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161+6018T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749493 | |||||||
chr2:48749496 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161+6015C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749496 | |||||||
chr2:48749641 | G | A | 1 | a0003c0003t0003g0348 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.161+5870C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749641 | |||||||
chr2:48749658 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.161+5853A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749658 | |||||||
chr2:48749720 | T | TA | 31 | a0001c0001t0001g0304 a0002c0002t0004g0068 a0002c0002t0008g0098 others(28): Show |
31 | HG00733.hp1 HG01071.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.161+5790dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749720 | |||||||
chr2:48749720 | TA | T | 72 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(69): Show |
75 | HG00280.hp2 HG00558.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.161+5790delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749720 | |||||||
chr2:48749736 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0142 others(5): Show |
8 | HG02027.hp2 HG02165.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+5775T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749736 | |||||||
chr2:48749742 | G | GA | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | NA19056.hp2 NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.161+5768dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749742 | |||||||
chr2:48749747 | A | C | 46 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(43): Show |
48 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.161+5764T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749747 | |||||||
chr2:48749831 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161+5680G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749831 | |||||||
chr2:48749876 | T | G | 1 | a0003c0003t0001g0358 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.161+5635A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749876 | |||||||
chr2:48749968 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.161+5543C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749968 | |||||||
chr2:48749981 | T | G | 75 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0102 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.161+5530A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749981 | |||||||
chr2:48750045 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG00408.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.161+5466T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750045 | |||||||
chr2:48750268 | T | C | 1 | a0001c0001t0001g0298 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.161+5243A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750268 | |||||||
chr2:48750488 | A | G | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.161+5023T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750488 | |||||||
chr2:48750639 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.161+4872G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750639 | |||||||
chr2:48750682 | A | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0089 others(30): Show |
36 | HG00558.hp2 HG00609.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.161+4829T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750682 | |||||||
chr2:48750810 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.161+4701G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750810 | |||||||
chr2:48750823 | G | A | 1 | a0003c0004t0001g0359 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.161+4688C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750823 | |||||||
chr2:48750970 | C | T | 6 | a0003c0003t0001g0330 a0003c0003t0001g0357 a0003c0003t0002g0340 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+4541G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750970 | |||||||
chr2:48751020 | A | G | 94 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(91): Show |
100 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.161+4491T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751020 | |||||||
chr2:48751125 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
166 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.161+4386G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751125 | |||||||
chr2:48751143 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.161+4368C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751143 | |||||||
chr2:48751178 | A | G | 1 | a0002c0002t0002g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.161+4333T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751178 | |||||||
chr2:48751253 | AT | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
175 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.161+4257delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751253 | |||||||
chr2:48751258 | T | G | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.161+4253A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751258 | |||||||
chr2:48751311 | C | A | 1 | a0001c0001t0001g0230 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.161+4200G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751311 | |||||||
chr2:48751335 | C | G | 12 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(9): Show |
12 | HG01109.hp1 HG01358.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.161+4176G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751335 | |||||||
chr2:48751626 | T | C | 28 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0299 others(25): Show |
28 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.161+3885A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751626 | |||||||
chr2:48751973 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0026 |
2 | NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.161+3538G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751973 | |||||||
chr2:48752141 | G | T | 1 | a0004c0007t0003g0316 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161+3370C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752141 | |||||||
chr2:48752356 | T | A | 4 | a0002c0002t0001g0261 a0002c0002t0001g0284 a0002c0002t0005g0250 others(1): Show |
4 | HG01109.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+3155A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752356 | |||||||
chr2:48752466 | T | C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | NA18940.hp1 NA18982.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+3045A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752466 | |||||||
chr2:48752493 | C | G | 5 | a0002c0002t0001g0295 a0002c0002t0001g0297 a0002c0002t0003g0097 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+3018G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752493 | |||||||
chr2:48752527 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.161+2984A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752527 | |||||||
chr2:48752529 | CT | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
263 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.161+2981delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752529 | |||||||
chr2:48752798 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.161+2713C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752798 | |||||||
chr2:48752864 | T | C | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+2647A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752864 | |||||||
chr2:48752981 | C | CG | 44 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0091 others(41): Show |
46 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.161+2529dupC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752981 | |||||||
chr2:48752981 | C | CGGGG | 20 | a0001c0001t0001g0007 a0001c0001t0001g0129 a0001c0001t0001g0130 others(17): Show |
21 | HG00642.hp1 HG00738.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.161+2526_161+2529d others(6): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752981 | |||||||
chr2:48752981 | C | CGGGGGGG others(5): Show |
1 | a0002c0002t0003g0128 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.161+2518_161+2529d others(14): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752981 | |||||||
chr2:48752981 | CG | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0062 others(29): Show |
34 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.161+2529delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752981 | |||||||
chr2:48752985 | G | C | 1 | a0003c0004t0001g0349 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.161+2526C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752985 | |||||||
chr2:48752986 | G | GA | 15 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
15 | HG00408.hp2 HG00544.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+2524_161+2525i others(3): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752986 | |||||||
chr2:48752986 | G | GGGGCGGG others(12): Show |
2 | a0003c0003t0001g0330 a0003c0003t0001g0357 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.161+2524_161+2525i others(21): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752986 | |||||||
chr2:48752986 | G | GGGGTGGG others(13): Show |
1 | a0003c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.161+2524_161+2525i others(22): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752986 | |||||||
chr2:48752986 | G | T | 2 | a0003c0004t0001g0332 a0003c0004t0001g0351 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.161+2525C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752986 | |||||||
chr2:48752987 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(45): Show |
52 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.161+2524C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752987 | |||||||
chr2:48752988 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0062 |
3 | HG00621.hp2 HG02040.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.161+2523C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752988 | |||||||
chr2:48752988 | G | T | 1 | a0002c0002t0002g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161+2523C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752988 | |||||||
chr2:48752991 | G | GGGGGGGG others(15): Show |
2 | a0001c0001t0001g0299 a0003c0004t0001g0333 |
2 | HG02523.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(24): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGGGG others(14): Show |
3 | a0003c0003t0003g0360 a0003c0003t0004g0334 a0003c0004t0001g0335 |
3 | HG01261.hp1 HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(23): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGGGT others(14): Show |
6 | a0001c0001t0001g0289 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01169.hp1 HG02056.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(23): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGGGT others(13): Show |
9 | a0001c0001t0001g0106 a0001c0001t0001g0300 a0003c0003t0004g0338 others(6): Show |
10 | HG00423.hp1 HG00639.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(22): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGGTG others(14): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0104 a0001c0001t0001g0105 |
4 | HG01099.hp1 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(23): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGGTG others(13): Show |
8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0321 others(5): Show |
8 | HG00735.hp1 HG01256.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(22): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGGTG others(12): Show |
11 | a0001c0001t0001g0301 a0001c0001t0001g0303 a0001c0001t0001g0304 others(8): Show |
11 | HG01243.hp2 HG01952.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(21): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGGTG others(9): Show |
3 | a0002c0002t0001g0295 a0002c0002t0004g0294 a0004c0007t0003g0296 |
3 | HG03209.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(18): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGTGG others(12): Show |
3 | a0001c0001t0001g0298 a0003c0003t0002g0355 a0003c0004t0001g0356 |
3 | HG01257.hp1 HG01496.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(21): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGGTGG others(11): Show |
13 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0309 others(10): Show |
13 | HG00280.hp1 HG01081.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(20): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGTGGG others(11): Show |
1 | a0002c0002t0002g0324 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.161+2519_161+2520i others(20): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGTGGG others(10): Show |
5 | a0002c0002t0002g0317 a0003c0003t0002g0346 a0003c0004t0001g0328 others(2): Show |
5 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(19): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGGTGGG others(7): Show |
1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+2519_161+2520i others(16): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGTGGGG others(9): Show |
2 | a0003c0003t0002g0347 a0003c0003t0003g0348 |
2 | HG01069.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(18): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GGGTGGGG others(6): Show |
1 | a0002c0002t0001g0297 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+2519_161+2520i others(15): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | GT | 5 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | HG02132.hp1 HG03834.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(3): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752991 | G | T | 3 | a0003c0003t0001g0330 a0003c0003t0001g0357 a0003c0004t0001g0350 |
3 | HG01515.hp2 HG01517.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.161+2520C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | |||||||
chr2:48752994 | G | T | 3 | a0002c0002t0001g0244 a0002c0002t0003g0245 a0002c0002t0004g0068 |
3 | HG02486.hp1 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.161+2517C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752994 | |||||||
chr2:48753017 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.161+2494G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753017 | |||||||
chr2:48753236 | A | G | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(346): Show |
362 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(359): Show |
intron_variant | MODIFIER | c.161+2275T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753236 | |||||||
chr2:48753368 | G | T | 67 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(64): Show |
69 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.161+2143C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753368 | |||||||
chr2:48753625 | A | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+1886T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753625 | |||||||
chr2:48753627 | A | T | 2 | a0002c0002t0001g0244 a0002c0002t0003g0245 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.161+1884T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753627 | |||||||
chr2:48753682 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+1829C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753682 | |||||||
chr2:48753799 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02040.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.161+1712T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753799 | |||||||
chr2:48753805 | A | AGT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0063 others(13): Show |
18 | HG00280.hp2 HG00741.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+1704_161+1705d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753805 | |||||||
chr2:48753805 | A | AGTGTGT | 71 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0102 others(68): Show |
73 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.161+1700_161+1705d others(8): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753805 | |||||||
chr2:48753805 | AGT | A | 69 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0071 others(66): Show |
72 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.161+1704_161+1705d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753805 | |||||||
chr2:48753913 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18941.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.161+1598G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753913 | |||||||
chr2:48754109 | A | G | 5 | a0002c0002t0001g0295 a0002c0002t0001g0297 a0002c0002t0003g0097 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+1402T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754109 | |||||||
chr2:48754173 | A | T | 3 | a0001c0001t0001g0111 a0002c0002t0003g0110 a0002c0002t0003g0112 |
3 | HG01243.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.161+1338T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754173 | |||||||
chr2:48754225 | A | G | 1 | a0003c0003t0003g0331 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161+1286T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754225 | |||||||
chr2:48754251 | A | G | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+1260T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754251 | |||||||
chr2:48754339 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0002c0002t0003g0064 others(1): Show |
6 | HG01433.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+1172C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754339 | |||||||
chr2:48754415 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0002c0002t0002g0109 |
3 | HG02572.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.161+1096G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754415 | |||||||
chr2:48754507 | A | G | 75 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0102 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.161+1004T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754507 | |||||||
chr2:48754595 | A | AC | 22 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0084 others(19): Show |
22 | HG01106.hp1 HG01261.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.161+915dupG | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754595 | |||||||
chr2:48754598 | C | A | 27 | a0001c0001t0001g0289 a0001c0001t0001g0299 a0001c0001t0001g0300 others(24): Show |
27 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.161+913G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754598 | |||||||
chr2:48754638 | A | G | 1 | a0003c0004t0001g0328 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.161+873T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754638 | |||||||
chr2:48754653 | C | T | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+858G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754653 | |||||||
chr2:48754758 | A | G | 16 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0002c0002t0001g0070 others(13): Show |
17 | HG01891.hp2 HG02145.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.161+753T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754758 | |||||||
chr2:48754822 | A | G | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+689T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754822 | |||||||
chr2:48754835 | C | T | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+676G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754835 | |||||||
chr2:48754902 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | HG02129.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.161+609C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754902 | |||||||
chr2:48754925 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.161+586C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754925 | |||||||
chr2:48754958 | CA | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.161+552delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754958 | |||||||
chr2:48754974 | C | T | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+537G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754974 | |||||||
chr2:48754993 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.161+518C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754993 | |||||||
chr2:48755011 | G | A | 3 | a0002c0002t0005g0326 a0003c0008t0004g0012 a0003c0008t0004g0361 |
4 | HG02896.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+500C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755011 | |||||||
chr2:48755035 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.161+476G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755035 | |||||||
chr2:48755123 | G | A | 2 | a0001c0001t0001g0292 a0002c0002t0003g0293 |
2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161+388C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755123 | |||||||
chr2:48755219 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(54): Show |
62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.161+292C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755219 | |||||||
chr2:48755346 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.161+165A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755346 | |||||||
chr2:48755483 | C | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(55): Show |
63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.161+28G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755483 | |||||||
chr2:48755494 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.161+17C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755494 |