Item | Value |
---|---|
geneid | 23240 |
ensemblid | ENSG00000121210.16 |
hgncid | 29146 |
symbol | TMEM131L |
name | transmembrane 131 like |
refseq_nuc | NM_001131007.2 |
refseq_prot | NP_001124479.1 |
ensembl_nuc | ENST00000409959.8 |
ensembl_prot | ENSP00000386787.3 |
mane_status | MANE Select |
chr | chr4 |
start | 153466360 |
end | 153636711 |
strand | + |
ver | v1.2 |
region | chr4:153466360-153636711 |
region5000 | chr4:153461360-153641711 |
regionname0 | TMEM131L_chr4_153466360_153636711 |
regionname5000 | TMEM131L_chr4_153461360_153641711 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1610 | 175 | 66 | 26 | 59 | 4 | 19 | 46 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0002 | 0/0 | 1610 | 47 | 11 | 10 | 21 | 2 | 3 | 16 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0003 | 0/0 | 1610 | 6 | 0 | 6 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0004 | 0/0 | 1610 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0005 | 0/0 | 1610 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0006 | 0/0 | 1610 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0007 | 0/1 | 1610 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0008 | 0/0 | 1610 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0009 | 0/0 | 1610 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0010 | 0/0 | 1610 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0011 | 0/0 | 1610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0012 | 0/0 | 1610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0013 | 0/0 | 1610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
a0014 | 0/0 | 1610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | MAGLR others(1605): Show |
chr4 | 153461360 | 153641711 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4830 | 32 | 26 | 1 | 3 | 0 | 2 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0002 | 0/0 | 4830 | 27 | 13 | 0 | 8 | 1 | 5 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0003 | 1/0 | 4830 | 21 | 2 | 5 | 7 | 1 | 5 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0004 | 0/0 | 4830 | 20 | 0 | 7 | 12 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0005 | 0/0 | 4830 | 14 | 11 | 2 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0008 | 0/0 | 4830 | 9 | 4 | 2 | 2 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0009 | 0/0 | 4830 | 8 | 0 | 1 | 7 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0011 | 0/0 | 4830 | 7 | 0 | 2 | 1 | 0 | 4 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0012 | 0/0 | 4830 | 7 | 0 | 2 | 5 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0013 | 0/0 | 4830 | 6 | 0 | 0 | 5 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0014 | 0/0 | 4830 | 6 | 0 | 3 | 3 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0020 | 0/0 | 4830 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0021 | 0/0 | 4830 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0022 | 0/0 | 4830 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0024 | 0/0 | 4830 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0026 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0028 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0030 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0033 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0034 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0037 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0041 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0047 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0056 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0001c0059 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0006 | 0/0 | 4830 | 12 | 2 | 0 | 8 | 1 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0007 | 0/0 | 4830 | 9 | 6 | 2 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0010 | 0/0 | 4830 | 7 | 2 | 3 | 2 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0015 | 0/0 | 4830 | 4 | 0 | 0 | 3 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0016 | 0/0 | 4830 | 4 | 0 | 2 | 1 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0025 | 0/0 | 4830 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0029 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0031 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0039 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0043 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0045 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0048 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0051 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0055 | 0/0 | 4830 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0002c0057 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0003c0019 | 0/0 | 4830 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0003c0023 | 0/0 | 4830 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0003c0054 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0004c0018 | 0/0 | 4830 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0004c0027 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0004c0036 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0005c0017 | 0/0 | 4830 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0006c0040 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0006c0050 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0007c0044 | 0/1 | 4830 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0007c0049 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0008c0046 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0008c0052 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0009c0053 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0010c0038 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0011c0035 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0012c0032 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0013c0058 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 | ||
a0014c0042 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | ATGGC others(4825): Show |
chr4 | 153461360 | 153641711 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5006 | 27 | 21 | 1 | 3 | 0 | 2 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0001t0002 | 0/0 | 5006 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0002t0001 | 0/0 | 5006 | 24 | 10 | 0 | 8 | 1 | 5 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0002t0002 | 0/0 | 5006 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0003t0001 | 1/0 | 5006 | 21 | 2 | 5 | 7 | 1 | 5 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0004t0001 | 0/0 | 5006 | 20 | 0 | 7 | 12 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0005t0001 | 0/0 | 5006 | 12 | 9 | 2 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0005t0002 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0005t0003 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0008t0001 | 0/0 | 5006 | 9 | 4 | 2 | 2 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0009t0001 | 0/0 | 5006 | 8 | 0 | 1 | 7 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0011t0001 | 0/0 | 5006 | 7 | 0 | 2 | 1 | 0 | 4 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0012t0001 | 0/0 | 5006 | 7 | 0 | 2 | 5 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0013t0001 | 0/0 | 5006 | 6 | 0 | 0 | 5 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0014t0001 | 0/0 | 5006 | 6 | 0 | 3 | 3 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0020t0001 | 0/0 | 5006 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0021t0001 | 0/0 | 5006 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0022t0001 | 0/0 | 5006 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0024t0001 | 0/0 | 5006 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0026t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0028t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0030t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0033t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0034t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0037t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0041t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0047t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0056t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0001c0059t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0006t0001 | 0/0 | 5006 | 12 | 2 | 0 | 8 | 1 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0007t0001 | 0/0 | 5006 | 9 | 6 | 2 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0010t0001 | 0/0 | 5006 | 7 | 2 | 3 | 2 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0015t0001 | 0/0 | 5006 | 4 | 0 | 0 | 3 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0016t0001 | 0/0 | 5006 | 4 | 0 | 2 | 1 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0025t0001 | 0/0 | 5006 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0029t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0031t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0039t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0043t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0045t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0048t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0051t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0055t0001 | 0/0 | 5006 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0002c0057t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0003c0019t0001 | 0/0 | 5006 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0003c0023t0001 | 0/0 | 5006 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0003c0054t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0004c0018t0001 | 0/0 | 5006 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0004c0027t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0004c0036t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0005c0017t0001 | 0/0 | 5006 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0006c0040t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0006c0050t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0007c0044t0001 | 0/1 | 5006 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0007c0049t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0008c0046t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0008c0052t0001 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0009c0053t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0010c0038t0001 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0011c0035t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0012c0032t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0013c0058t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
a0014c0042t0001 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | GAGCG others(5001): Show |
chr4 | 153461360 | 153641711 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0005t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0008t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0009t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0009t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0009t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0009t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0009t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0009t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0009t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0009t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0011t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0011t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0011t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0011t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0011t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0011t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0012t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0012t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0012t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0012t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0012t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0012t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0012t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0013t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0013t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0013t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0013t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0013t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0013t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0014t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0014t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0014t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0014t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0014t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0014t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0020t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0020t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0021t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0021t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0022t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0022t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0024t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0024t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0026t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0028t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0030t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0033t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0034t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0037t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0041t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0047t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0056t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0001c0059t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0007t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0010t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0010t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0010t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0010t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0010t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0010t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0010t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0015t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0015t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0015t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0016t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0016t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0016t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0016t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0025t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0025t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0029t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0031t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0039t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0043t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0045t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0048t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0051t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0055t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0002c0057t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0003c0019t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0003c0019t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0003c0019t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0003c0023t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0003c0023t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0003c0054t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0004c0018t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0004c0018t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0004c0018t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0004c0027t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0004c0036t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0005c0017t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0005c0017t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0005c0017t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0006c0040t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0006c0050t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0007c0044t0001g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0007c0049t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0008c0046t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0008c0052t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0009c0053t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0010c0038t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0011c0035t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0012c0032t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0013c0058t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
a0014c0042t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0004 | t0001 | g0125 | EUR | GBR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0182 | EUR | GBR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00408 | hp1 | a0001 | c0012 | t0001 | g0149 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0161 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00544 | hp2 | a0001 | c0012 | t0001 | g0156 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00558 | hp1 | a0002 | c0016 | t0001 | g0139 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00558 | hp2 | a0002 | c0010 | t0001 | g0069 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00597 | hp1 | a0001 | c0013 | t0001 | g0044 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00597 | hp2 | a0001 | c0009 | t0001 | g0158 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00609 | hp1 | a0002 | c0006 | t0001 | g0132 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00609 | hp2 | a0001 | c0004 | t0001 | g0171 | EAS | CHS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0196 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG00735 | hp2 | a0002 | c0010 | t0001 | g0016 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01070 | hp1 | a0001 | c0011 | t0001 | g0105 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01070 | hp2 | a0002 | c0010 | t0001 | g0075 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01071 | hp1 | a0001 | c0008 | t0001 | g0184 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01071 | hp2 | a0002 | c0010 | t0001 | g0073 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01081 | hp1 | a0002 | c0016 | t0001 | g0216 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01081 | hp2 | a0001 | c0005 | t0001 | g0111 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01099 | hp1 | a0002 | c0045 | t0001 | g0121 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01099 | hp2 | a0001 | c0012 | t0001 | g0126 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01109 | hp2 | a0001 | c0005 | t0001 | g0109 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01192 | hp1 | a0001 | c0008 | t0001 | g0199 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01192 | hp2 | a0010 | c0038 | t0001 | g0056 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01243 | hp1 | a0002 | c0043 | t0001 | g0209 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01255 | hp1 | a0004 | c0018 | t0001 | g0003 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01255 | hp2 | a0006 | c0040 | t0001 | g0030 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01257 | hp1 | a0003 | c0023 | t0001 | g0083 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01257 | hp2 | a0002 | c0007 | t0001 | g0071 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01258 | hp1 | a0002 | c0016 | t0001 | g0215 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01258 | hp2 | a0002 | c0007 | t0001 | g0072 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01346 | hp1 | a0007 | c0049 | t0001 | g0195 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01346 | hp2 | a0001 | c0004 | t0001 | g0134 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01361 | hp1 | a0001 | c0004 | t0001 | g0140 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0167 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01496 | hp1 | a0001 | c0014 | t0001 | g0138 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01496 | hp2 | a0001 | c0012 | t0001 | g0205 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01516 | hp1 | a0002 | c0006 | t0001 | g0185 | EUR | IBS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01516 | hp2 | a0001 | c0022 | t0001 | g0078 | EUR | IBS | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01884 | hp1 | a0002 | c0006 | t0001 | g0202 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01884 | hp2 | a0001 | c0028 | t0001 | g0108 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01928 | hp1 | a0001 | c0004 | t0001 | g0152 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01928 | hp2 | a0003 | c0019 | t0001 | g0154 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01934 | hp1 | a0001 | c0004 | t0001 | g0127 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01934 | hp2 | a0001 | c0011 | t0001 | g0110 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01978 | hp1 | a0003 | c0054 | t0001 | g0123 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0133 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01993 | hp1 | a0001 | c0022 | t0001 | g0114 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01993 | hp2 | a0003 | c0019 | t0001 | g0153 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02004 | hp1 | a0001 | c0003 | t0001 | g0119 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0115 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02055 | hp1 | a0001 | c0005 | t0001 | g0218 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02071 | hp2 | a0002 | c0006 | t0001 | g0200 | EAS | KHV | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02135 | hp1 | a0001 | c0004 | t0001 | g0212 | EAS | KHV | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02135 | hp2 | a0002 | c0010 | t0001 | g0085 | EAS | KHV | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02145 | hp1 | a0001 | c0033 | t0001 | g0099 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02145 | hp2 | a0001 | c0021 | t0001 | g0014 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02148 | hp1 | a0003 | c0023 | t0001 | g0107 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02148 | hp2 | a0001 | c0004 | t0001 | g0143 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02257 | hp1 | a0001 | c0005 | t0002 | g0064 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0183 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02273 | hp1 | a0003 | c0019 | t0001 | g0198 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02273 | hp2 | a0001 | c0014 | t0001 | g0155 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02280 | hp1 | a0001 | c0024 | t0001 | g0010 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02293 | hp1 | a0001 | c0009 | t0001 | g0177 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02293 | hp2 | a0001 | c0004 | t0001 | g0142 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02300 | hp1 | a0001 | c0014 | t0001 | g0144 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02300 | hp2 | a0006 | c0050 | t0001 | g0116 | AMR | PEL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02523 | hp1 | a0001 | c0014 | t0001 | g0174 | EAS | KHV | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02523 | hp2 | a0001 | c0026 | t0001 | g0077 | EAS | KHV | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02572 | hp2 | a0001 | c0021 | t0001 | g0037 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02615 | hp1 | a0005 | c0017 | t0001 | g0040 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02615 | hp2 | a0011 | c0035 | t0001 | g0035 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02622 | hp2 | a0002 | c0007 | t0001 | g0231 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02630 | hp2 | a0001 | c0041 | t0001 | g0220 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02647 | hp2 | a0002 | c0007 | t0001 | g0228 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0178 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02683 | hp2 | a0001 | c0011 | t0001 | g0112 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0238 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02809 | hp2 | a0002 | c0007 | t0001 | g0096 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02886 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02886 | hp2 | a0012 | c0032 | t0001 | g0036 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02895 | hp2 | a0005 | c0017 | t0001 | g0026 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02896 | hp1 | a0001 | c0005 | t0001 | g0221 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02897 | hp2 | a0005 | c0017 | t0001 | g0027 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02922 | hp1 | a0001 | c0008 | t0001 | g0128 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02922 | hp2 | a0002 | c0057 | t0001 | g0032 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02965 | hp1 | a0001 | c0024 | t0001 | g0015 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02970 | hp1 | a0001 | c0005 | t0001 | g0247 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02976 | hp1 | a0001 | c0008 | t0001 | g0204 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03017 | hp2 | a0002 | c0015 | t0001 | g0241 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03041 | hp1 | a0001 | c0059 | t0001 | g0033 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03098 | hp2 | a0004 | c0036 | t0001 | g0234 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03139 | hp1 | a0001 | c0005 | t0001 | g0038 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03139 | hp2 | a0004 | c0018 | t0001 | g0101 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03195 | hp2 | a0002 | c0010 | t0001 | g0021 | AFR | ESN | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03209 | hp1 | a0013 | c0058 | t0001 | g0031 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03209 | hp2 | a0001 | c0005 | t0001 | g0232 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03225 | hp1 | a0002 | c0007 | t0001 | g0023 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03225 | hp2 | a0014 | c0042 | t0001 | g0001 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0065 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03490 | hp1 | a0001 | c0011 | t0001 | g0079 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0201 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03491 | hp2 | a0001 | c0011 | t0001 | g0243 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03540 | hp1 | a0001 | c0005 | t0001 | g0022 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | GWD | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03579 | hp1 | a0002 | c0007 | t0001 | g0070 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03654 | hp1 | a0002 | c0006 | t0001 | g0242 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03704 | hp1 | a0001 | c0020 | t0001 | g0074 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03704 | hp2 | a0002 | c0016 | t0001 | g0191 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03710 | hp2 | a0001 | c0008 | t0001 | g0194 | SAS | PJL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03831 | hp1 | a0001 | c0011 | t0001 | g0048 | SAS | BEB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0181 | SAS | BEB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0122 | SAS | BEB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG04199 | hp1 | a0001 | c0013 | t0001 | g0088 | SAS | STU | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | STU | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | STU | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0239 | SAS | STU | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18522 | hp1 | a0004 | c0018 | t0001 | g0029 | AFR | YRI | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18522 | hp2 | a0001 | c0037 | t0001 | g0230 | AFR | YRI | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | CHB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18747 | hp2 | a0001 | c0012 | t0001 | g0131 | EAS | CHB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18906 | hp2 | a0001 | c0034 | t0001 | g0020 | AFR | YRI | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18940 | hp1 | a0002 | c0048 | t0001 | g0168 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18940 | hp2 | a0002 | c0007 | t0001 | g0084 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18942 | hp2 | a0001 | c0009 | t0001 | g0190 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18943 | hp1 | a0001 | c0009 | t0001 | g0104 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18943 | hp2 | a0008 | c0052 | t0001 | g0120 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18944 | hp1 | a0001 | c0004 | t0001 | g0189 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18950 | hp1 | a0002 | c0025 | t0001 | g0103 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18950 | hp2 | a0001 | c0004 | t0001 | g0214 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18952 | hp1 | a0001 | c0013 | t0001 | g0090 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18952 | hp2 | a0002 | c0025 | t0001 | g0166 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18953 | hp1 | a0001 | c0004 | t0001 | g0137 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18960 | hp1 | a0001 | c0030 | t0001 | g0093 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18960 | hp2 | a0001 | c0004 | t0001 | g0146 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18963 | hp1 | a0001 | c0013 | t0001 | g0087 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18963 | hp2 | a0001 | c0004 | t0001 | g0197 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18971 | hp1 | a0001 | c0009 | t0001 | g0145 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18971 | hp2 | a0001 | c0008 | t0001 | g0187 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18972 | hp1 | a0002 | c0006 | t0001 | g0130 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18978 | hp1 | a0001 | c0009 | t0001 | g0175 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18978 | hp2 | a0002 | c0015 | t0001 | g0018 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18979 | hp2 | a0001 | c0047 | t0001 | g0159 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18981 | hp1 | a0002 | c0006 | t0001 | g0164 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18981 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18983 | hp1 | a0001 | c0014 | t0001 | g0150 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18986 | hp1 | a0001 | c0009 | t0001 | g0170 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18986 | hp2 | a0002 | c0031 | t0001 | g0043 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18989 | hp1 | a0001 | c0020 | t0001 | g0094 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18989 | hp2 | a0001 | c0004 | t0001 | g0148 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18991 | hp1 | a0001 | c0005 | t0001 | g0055 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18991 | hp2 | a0001 | c0056 | t0001 | g0160 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18994 | hp1 | a0002 | c0006 | t0001 | g0210 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18994 | hp2 | a0002 | c0006 | t0001 | g0118 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19002 | hp1 | a0001 | c0013 | t0001 | g0049 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19010 | hp2 | a0001 | c0008 | t0001 | g0136 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19011 | hp2 | a0002 | c0015 | t0001 | g0046 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19043 | hp1 | a0001 | c0005 | t0003 | g0034 | AFR | LWK | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19043 | hp2 | a0004 | c0027 | t0001 | g0248 | AFR | LWK | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19060 | hp1 | a0002 | c0006 | t0001 | g0165 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19060 | hp2 | a0001 | c0014 | t0001 | g0211 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19065 | hp1 | a0002 | c0015 | t0001 | g0151 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19065 | hp2 | a0001 | c0009 | t0001 | g0192 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19070 | hp1 | a0002 | c0051 | t0001 | g0102 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19070 | hp2 | a0008 | c0046 | t0001 | g0188 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19075 | hp1 | a0002 | c0039 | t0001 | g0053 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19075 | hp2 | a0001 | c0004 | t0001 | g0135 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19077 | hp1 | a0001 | c0004 | t0001 | g0240 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19077 | hp2 | a0001 | c0013 | t0001 | g0052 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19082 | hp1 | a0001 | c0011 | t0001 | g0050 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19082 | hp2 | a0001 | c0004 | t0001 | g0193 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19084 | hp2 | a0002 | c0006 | t0001 | g0186 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19086 | hp1 | a0001 | c0012 | t0001 | g0169 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ASW | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0060 | EUR | TSI | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA20752 | hp2 | a0002 | c0055 | t0001 | g0207 | EUR | TSI | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01123 | hp1 | a0002 | c0029 | t0001 | g0067 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG01123 | hp2 | a0009 | c0053 | t0001 | g0179 | AMR | CLM | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02109 | hp1 | a0001 | c0008 | t0001 | g0129 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02109 | hp2 | a0002 | c0010 | t0001 | g0028 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02486 | hp1 | a0002 | c0006 | t0001 | g0203 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02559 | hp1 | a0002 | c0007 | t0001 | g0229 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0206 | AFR | ACB | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03471 | hp1 | a0001 | c0005 | t0001 | g0106 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | USA | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18955 | hp1 | a0001 | c0012 | t0001 | g0162 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA18955 | hp2 | a0001 | c0004 | t0001 | g0147 | EAS | JPT | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | USA | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
NA20300 | hp2 | a0001 | c0008 | t0001 | g0176 | AFR | USA | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
homoSapiens | chm13v2 | a0007 | c0044 | t0001 | g0208 | REF | REF | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0180 | REF | REF | TMEM131L_chr4_153461360_153641711 | TMEM131L | chr4 | 153461360 | 153641711 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:153467220 | C | G | 1 | a0014 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.134C>G | p.Pro45Arg | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/35 | 172/5006 | 134/4833 | 45/1610 | chr4 | 153467220 | |||
chr4:153581414 | A | G | 1 | a0005 | 3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.746A>G | p.Tyr249Cys | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/35 | 784/5006 | 746/4833 | 249/1610 | chr4 | 153581414 | |||
chr4:153581503 | C | G | 1 | a0005 | 3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.835C>G | p.His279Asp | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/35 | 873/5006 | 835/4833 | 279/1610 | chr4 | 153581503 | |||
chr4:153591177 | G | A | 1 | a0012 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1795G>A | p.Ala599Thr | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/35 | 1833/5006 | 1795/4833 | 599/1610 | chr4 | 153591177 | |||
chr4:153592475 | A | G | 6 | a0002 a0006 a0007 others(3): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
missense_variant&splice_region_variant | MODERATE | c.1813A>G | p.Ile605Val | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/35 | 1851/5006 | 1813/4833 | 605/1610 | chr4 | 153592475 | |||
chr4:153593813 | T | C | 6 | a0002 a0006 a0007 others(3): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
missense_variant | MODERATE | c.1937T>C | p.Met646Thr | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/35 | 1975/5006 | 1937/4833 | 646/1610 | chr4 | 153593813 | |||
chr4:153602253 | T | C | 1 | a0008 | 2 | NA18943.hp2 NA19070.hp2 |
missense_variant | MODERATE | c.2368T>C | p.Tyr790His | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 22/35 | 2406/5006 | 2368/4833 | 790/1610 | chr4 | 153602253 | |||
chr4:153602702 | T | C | 1 | a0010 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.2614T>C | p.Trp872Arg | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 23/35 | 2652/5006 | 2614/4833 | 872/1610 | chr4 | 153602702 | |||
chr4:153603986 | A | G | 2 | a0003 a0006 |
8 | HG01255.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
missense_variant | MODERATE | c.2974A>G | p.Thr992Ala | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/35 | 3012/5006 | 2974/4833 | 992/1610 | chr4 | 153603986 | |||
chr4:153612354 | C | G | 1 | a0009 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.3521C>G | p.Ser1174Cys | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/35 | 3559/5006 | 3521/4833 | 1174/1610 | chr4 | 153612354 | |||
chr4:153621753 | A | G | 1 | a0004 | 2 | HG03098.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.3763A>G | p.Asn1255Asp | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/35 | 3801/5006 | 3763/4833 | 1255/1610 | chr4 | 153621753 | |||
chr4:153621754 | A | G | 2 | a0004 a0013 |
6 | HG01255.hp1 HG03098.hp2 HG03139.hp2 others(3): Show |
missense_variant | MODERATE | c.3764A>G | p.Asn1255Ser | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/35 | 3802/5006 | 3764/4833 | 1255/1610 | chr4 | 153621754 | |||
chr4:153636464 | C | T | 2 | a0007 a0011 |
2 | HG01346.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.4721C>T | p.Pro1574Leu | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 35/35 | 4759/5006 | 4721/4833 | 1574/1610 | chr4 | 153636464 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:153466430 | C | T | 3 | a0001c0059 a0002c0057 a0013c0058 |
3 | HG02922.hp2 HG03041.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.33C>T | p.Cys11Cys | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/35 | 71/5006 | 33/4833 | 11/1610 | chr4 | 153466430 | |||
chr4:153466445 | G | C | 35 | a0001c0001 a0001c0002 a0001c0005 others(32): Show |
142 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(139): Show |
synonymous_variant | LOW | c.48G>C | p.Ala16Ala | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/35 | 86/5006 | 48/4833 | 16/1610 | chr4 | 153466445 | |||
chr4:153557070 | C | T | 30 | a0001c0001 a0001c0004 a0001c0009 others(27): Show |
118 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(115): Show |
synonymous_variant | LOW | c.537C>T | p.Val179Val | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/35 | 575/5006 | 537/4833 | 179/1610 | chr4 | 153557070 | |||
chr4:153558278 | T | C | 41 | a0001c0001 a0001c0004 a0001c0005 others(38): Show |
167 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(164): Show |
synonymous_variant | LOW | c.570T>C | p.Arg190Arg | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/35 | 608/5006 | 570/4833 | 190/1610 | chr4 | 153558278 | |||
chr4:153580850 | T | C | 4 | a0001c0030 a0002c0025 a0002c0031 others(1): Show |
5 | NA18950.hp1 NA18952.hp2 NA18960.hp1 others(2): Show |
synonymous_variant | LOW | c.685T>C | p.Leu229Leu | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/35 | 723/5006 | 685/4833 | 229/1610 | chr4 | 153580850 | |||
chr4:153584929 | G | A | 2 | a0002c0043 a0002c0045 |
2 | HG01099.hp1 HG01243.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1155G>A | p.Gln385Gln | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 12/35 | 1193/5006 | 1155/4833 | 385/1610 | chr4 | 153584929 | |||
chr4:153592570 | C | T | 21 | a0002c0006 a0002c0007 a0002c0010 others(18): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
synonymous_variant | LOW | c.1908C>T | p.His636His | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/35 | 1946/5006 | 1908/4833 | 636/1610 | chr4 | 153592570 | |||
chr4:153596293 | C | G | 1 | a0001c0028 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.2031C>G | p.Leu677Leu | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/35 | 2069/5006 | 2031/4833 | 677/1610 | chr4 | 153596293 | |||
chr4:153602668 | C | T | 1 | a0001c0047 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.2580C>T | p.Asp860Asp | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 23/35 | 2618/5006 | 2580/4833 | 860/1610 | chr4 | 153602668 | |||
chr4:153603366 | C | T | 1 | a0002c0043 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.2703C>T | p.Phe901Phe | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 24/35 | 2741/5006 | 2703/4833 | 901/1610 | chr4 | 153603366 | |||
chr4:153604108 | C | T | 1 | a0005c0017 | 3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.3096C>T | p.Ser1032Ser | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/35 | 3134/5006 | 3096/4833 | 1032/1610 | chr4 | 153604108 | |||
chr4:153604294 | A | C | 3 | a0001c0021 a0001c0037 a0001c0041 |
4 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
synonymous_variant | LOW | c.3282A>C | p.Ser1094Ser | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/35 | 3320/5006 | 3282/4833 | 1094/1610 | chr4 | 153604294 | |||
chr4:153604306 | C | T | 8 | a0001c0004 a0001c0011 a0001c0012 others(5): Show |
50 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(47): Show |
synonymous_variant | LOW | c.3294C>T | p.Ala1098Ala | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/35 | 3332/5006 | 3294/4833 | 1098/1610 | chr4 | 153604306 | |||
chr4:153620773 | G | A | 1 | a0002c0051 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.3585G>A | p.Arg1195Arg | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 27/35 | 3623/5006 | 3585/4833 | 1195/1610 | chr4 | 153620773 | |||
chr4:153623058 | G | A | 1 | a0001c0033 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.4020G>A | p.Val1340Val | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/35 | 4058/5006 | 4020/4833 | 1340/1610 | chr4 | 153623058 | |||
chr4:153623079 | G | A | 1 | a0001c0034 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.4041G>A | p.Pro1347Pro | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/35 | 4079/5006 | 4041/4833 | 1347/1610 | chr4 | 153623079 | |||
chr4:153627665 | C | T | 1 | a0001c0026 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.4185C>T | p.Pro1395Pro | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/35 | 4223/5006 | 4185/4833 | 1395/1610 | chr4 | 153627665 | |||
chr4:153632725 | C | T | 3 | a0001c0022 a0003c0019 a0003c0023 |
7 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(4): Show |
synonymous_variant | LOW | c.4215C>T | p.Tyr1405Tyr | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/35 | 4253/5006 | 4215/4833 | 1405/1610 | chr4 | 153632725 | |||
chr4:153632758 | G | T | 1 | a0002c0055 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.4248G>T | p.Val1416Val | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/35 | 4286/5006 | 4248/4833 | 1416/1610 | chr4 | 153632758 | |||
chr4:153632821 | G | A | 1 | a0002c0029 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.4311G>A | p.Ser1437Ser | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/35 | 4349/5006 | 4311/4833 | 1437/1610 | chr4 | 153632821 | |||
chr4:153636495 | C | T | 1 | a0002c0039 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.4752C>T | p.Asn1584Asn | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 35/35 | 4790/5006 | 4752/4833 | 1584/1610 | chr4 | 153636495 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:153466376 | G | C | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0005t0002 |
9 | HG02257.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/35 | 22 | chr4 | 153466376 | ||||||
chr4:153636698 | A | T | 1 | a0001c0005t0003 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 35/35 | 122 | chr4 | 153636698 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:153466545 | G | A | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124+24G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466545 | |||||||
chr4:153466547 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(12): Show |
15 | HG00735.hp2 HG01255.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+26T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466547 | |||||||
chr4:153466656 | G | A | 12 | a0001c0001t0001g0025 a0001c0002t0001g0017 a0001c0002t0001g0019 others(9): Show |
12 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.124+135G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466656 | |||||||
chr4:153466657 | A | G | 8 | a0001c0001t0001g0025 a0001c0002t0001g0024 a0001c0005t0001g0022 others(5): Show |
8 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+136A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466657 | |||||||
chr4:153466693 | C | G | 5 | a0001c0005t0001g0247 a0001c0034t0001g0020 a0004c0027t0001g0248 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+172C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466693 | |||||||
chr4:153466801 | C | A | 3 | a0001c0005t0001g0022 a0002c0007t0001g0023 a0002c0010t0001g0021 |
3 | HG03195.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.124+280C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466801 | |||||||
chr4:153466810 | C | T | 3 | a0001c0001t0001g0244 a0001c0002t0001g0245 a0001c0002t0001g0246 |
3 | HG02896.hp2 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.124+289C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466810 | |||||||
chr4:153466840 | C | T | 1 | a0001c0011t0001g0243 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.124+319C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466840 | |||||||
chr4:153466887 | C | G | 1 | a0002c0006t0001g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.125-324C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153466887 | |||||||
chr4:153467040 | C | T | 1 | a0002c0015t0001g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.125-171C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 1/34 | chr4 | 153467040 | |||||||
chr4:153467409 | G | C | 2 | a0001c0005t0001g0247 a0004c0027t0001g0248 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.195+128G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153467409 | |||||||
chr4:153467511 | G | A | 2 | a0002c0010t0001g0028 a0004c0018t0001g0029 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.195+230G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153467511 | |||||||
chr4:153467550 | G | C | 1 | a0001c0002t0001g0002 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.195+269G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153467550 | |||||||
chr4:153467794 | G | T | 1 | a0001c0004t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.195+513G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153467794 | |||||||
chr4:153467808 | A | G | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.195+527A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153467808 | |||||||
chr4:153467938 | A | G | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.195+657A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153467938 | |||||||
chr4:153468097 | C | A | 1 | a0006c0040t0001g0030 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.195+816C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153468097 | |||||||
chr4:153468378 | G | GC | 22 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 others(19): Show |
22 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.195+1101dupC | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153468378 | ||||||
chr4:153468432 | A | G | 1 | a0002c0016t0001g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.195+1151A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153468432 | |||||||
chr4:153468465 | C | CAT | 130 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(127): Show |
130 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(127): Show |
intron_variant | MODIFIER | c.195+1185_195+1186d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153468465 | ||||||
chr4:153468501 | A | G | 67 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0042 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.195+1220A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153468501 | |||||||
chr4:153468634 | C | G | 130 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(127): Show |
130 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(127): Show |
intron_variant | MODIFIER | c.195+1353C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153468634 | |||||||
chr4:153468809 | A | G | 3 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0015t0001g0018 |
3 | HG03017.hp1 HG04199.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.195+1528A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153468809 | |||||||
chr4:153468850 | G | A | 22 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 others(19): Show |
22 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.195+1569G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153468850 | |||||||
chr4:153469122 | T | C | 3 | a0001c0009t0001g0104 a0002c0025t0001g0103 a0002c0051t0001g0102 |
3 | NA18943.hp1 NA18950.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.195+1841T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153469122 | |||||||
chr4:153469235 | A | G | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.195+1954A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153469235 | |||||||
chr4:153469298 | GC | G | 114 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(111): Show |
114 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.195+2020delC | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469298 | ||||||
chr4:153469314 | G | GAC | 11 | a0001c0001t0001g0039 a0001c0003t0001g0117 a0001c0003t0001g0119 others(8): Show |
11 | HG01099.hp1 HG01243.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+2058_195+2059d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469314 | G | GACACAC | 9 | a0001c0002t0001g0113 a0001c0005t0001g0106 a0001c0005t0001g0109 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+2054_195+2059d others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469314 | G | GACACACA others(1): Show |
12 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0002t0001g0019 others(9): Show |
12 | HG01070.hp1 HG03017.hp1 HG04199.hp1 others(9): Show |
intron_variant | MODIFIER | c.195+2052_195+2059d others(10): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469314 | G | GACACACA others(3): Show |
38 | a0001c0001t0001g0025 a0001c0001t0002g0061 a0001c0001t0002g0062 others(35): Show |
38 | HG00558.hp2 HG00735.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2050_195+2059d others(12): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469314 | G | GACACACA others(5): Show |
31 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0042 others(28): Show |
31 | HG00597.hp1 HG01192.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.195+2048_195+2059d others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469314 | G | GACACACA others(7): Show |
25 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0041 others(22): Show |
25 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+2046_195+2059d others(16): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469314 | G | GACACACA others(9): Show |
18 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 others(15): Show |
18 | HG01255.hp1 HG02630.hp2 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+2044_195+2059d others(18): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469314 | G | GACACACA others(11): Show |
3 | a0001c0002t0001g0024 a0001c0002t0001g0217 a0001c0005t0001g0218 |
3 | HG01891.hp1 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.195+2042_195+2059d others(20): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469314 | GACAC | G | 3 | a0001c0002t0001g0213 a0001c0004t0001g0214 a0002c0016t0001g0215 |
3 | HG00544.hp1 HG01258.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.195+2056_195+2059d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469314 | ||||||
chr4:153469812 | G | A | 1 | a0001c0003t0001g0122 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.195+2531G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153469812 | |||||||
chr4:153469858 | G | A | 9 | a0001c0001t0001g0244 a0001c0002t0001g0017 a0001c0002t0001g0019 others(6): Show |
9 | HG02615.hp2 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+2577G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153469858 | |||||||
chr4:153469929 | A | AAAAC | 18 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 others(15): Show |
18 | HG02055.hp1 HG02486.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+2672_195+2675d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469929 | ||||||
chr4:153469929 | AAAAC | A | 61 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(58): Show |
61 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.195+2672_195+2675d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469929 | ||||||
chr4:153469953 | CAAA | C | 5 | a0001c0002t0001g0024 a0001c0005t0001g0247 a0004c0027t0001g0248 others(2): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+2677_195+2679d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153469953 | ||||||
chr4:153470031 | T | G | 1 | a0001c0003t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.195+2750T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470031 | |||||||
chr4:153470286 | C | T | 2 | a0005c0017t0001g0026 a0005c0017t0001g0027 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.195+3005C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470286 | |||||||
chr4:153470288 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(79): Show |
82 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.195+3007A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470288 | |||||||
chr4:153470340 | G | T | 40 | a0001c0001t0001g0039 a0001c0001t0001g0219 a0001c0001t0001g0222 others(37): Show |
40 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(37): Show |
intron_variant | MODIFIER | c.195+3059G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470340 | |||||||
chr4:153470462 | CAT | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(20): Show |
23 | HG00735.hp2 HG01255.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+3182_195+3183d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470462 | |||||||
chr4:153470579 | C | T | 1 | a0001c0005t0001g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-3266C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470579 | |||||||
chr4:153470738 | G | A | 40 | a0001c0001t0001g0039 a0001c0001t0001g0219 a0001c0001t0001g0222 others(37): Show |
40 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(37): Show |
intron_variant | MODIFIER | c.196-3107G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470738 | |||||||
chr4:153470833 | G | A | 6 | a0001c0005t0001g0022 a0001c0059t0001g0033 a0002c0007t0001g0023 others(3): Show |
6 | HG02922.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-3012G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470833 | |||||||
chr4:153470972 | C | T | 4 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-2873C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153470972 | |||||||
chr4:153470992 | C | CT | 84 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(81): Show |
84 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.196-2841dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153470992 | ||||||
chr4:153470992 | C | CTT | 37 | a0001c0001t0001g0039 a0001c0001t0001g0219 a0001c0001t0001g0222 others(34): Show |
37 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(34): Show |
intron_variant | MODIFIER | c.196-2842_196-2841d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153470992 | ||||||
chr4:153471010 | T | C | 2 | a0002c0010t0001g0028 a0004c0018t0001g0029 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.196-2835T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153471010 | |||||||
chr4:153471056 | C | T | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196-2789C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153471056 | |||||||
chr4:153471246 | A | T | 3 | a0001c0004t0001g0212 a0001c0014t0001g0211 a0002c0006t0001g0210 |
3 | HG02135.hp1 NA18994.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.196-2599A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153471246 | |||||||
chr4:153471353 | G | T | 1 | a0002c0010t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.196-2492G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153471353 | |||||||
chr4:153471526 | A | G | 12 | a0001c0001t0001g0039 a0001c0005t0001g0022 a0001c0005t0001g0038 others(9): Show |
12 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-2319A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153471526 | |||||||
chr4:153471721 | C | A | 5 | a0001c0002t0001g0024 a0001c0005t0001g0247 a0004c0027t0001g0248 others(2): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-2124C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153471721 | |||||||
chr4:153472077 | T | TA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(12): Show |
15 | HG00735.hp2 HG01255.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.196-1759dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153472077 | ||||||
chr4:153472291 | T | C | 5 | a0001c0002t0001g0024 a0001c0005t0001g0247 a0004c0027t0001g0248 others(2): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-1554T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153472291 | |||||||
chr4:153472358 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.196-1487A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153472358 | |||||||
chr4:153472358 | AG | A | 3 | a0001c0003t0001g0122 a0001c0004t0001g0125 a0001c0012t0001g0126 |
3 | HG00140.hp1 HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.196-1483delG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr4 | 153472358 | ||||||
chr4:153472640 | C | T | 1 | a0001c0002t0001g0057 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.196-1205C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153472640 | |||||||
chr4:153472653 | T | C | 1 | a0001c0004t0001g0127 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.196-1192T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153472653 | |||||||
chr4:153472674 | G | C | 3 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0015t0001g0018 |
3 | HG03017.hp1 HG04199.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.196-1171G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153472674 | |||||||
chr4:153472783 | C | G | 6 | a0001c0005t0001g0022 a0001c0059t0001g0033 a0002c0007t0001g0023 others(3): Show |
6 | HG02922.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-1062C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153472783 | |||||||
chr4:153472851 | A | T | 1 | a0002c0043t0001g0209 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196-994A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153472851 | |||||||
chr4:153472932 | T | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-913T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153472932 | |||||||
chr4:153473044 | C | T | 2 | a0001c0020t0001g0094 a0001c0030t0001g0093 |
2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.196-801C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473044 | |||||||
chr4:153473133 | G | T | 3 | a0001c0003t0001g0124 a0002c0045t0001g0121 a0002c0055t0001g0207 |
3 | HG01099.hp1 HG01109.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.196-712G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473133 | |||||||
chr4:153473211 | A | G | 1 | a0001c0002t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196-634A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473211 | |||||||
chr4:153473296 | T | G | 2 | a0001c0001t0001g0042 a0002c0031t0001g0043 |
2 | NA18986.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.196-549T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473296 | |||||||
chr4:153473442 | G | T | 3 | a0001c0005t0003g0034 a0011c0035t0001g0035 a0012c0032t0001g0036 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.196-403G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473442 | |||||||
chr4:153473637 | C | A | 1 | a0001c0005t0001g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196-208C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473637 | |||||||
chr4:153473661 | A | G | 1 | a0001c0003t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.196-184A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473661 | |||||||
chr4:153473697 | C | T | 1 | a0002c0007t0001g0084 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.196-148C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473697 | |||||||
chr4:153473706 | T | C | 1 | a0002c0007t0001g0084 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.196-139T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 2/34 | chr4 | 153473706 | |||||||
chr4:153473927 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0002t0001g0002 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+39G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153473927 | |||||||
chr4:153474039 | T | G | 2 | a0001c0008t0001g0128 a0001c0008t0001g0129 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.239+151T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474039 | |||||||
chr4:153474072 | G | GTTGT | 11 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(8): Show |
11 | HG02055.hp1 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.239+187_239+190dup others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153474072 | ||||||
chr4:153474158 | G | A | 34 | a0001c0003t0001g0133 a0001c0003t0001g0141 a0001c0004t0001g0115 others(31): Show |
34 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.239+270G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474158 | |||||||
chr4:153474399 | G | A | 12 | a0001c0003t0001g0157 a0001c0003t0001g0161 a0001c0003t0001g0163 others(9): Show |
12 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.239+511G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474399 | |||||||
chr4:153474402 | A | G | 1 | a0001c0012t0001g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.239+514A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474402 | |||||||
chr4:153474629 | C | G | 1 | a0008c0052t0001g0120 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.239+741C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474629 | |||||||
chr4:153474654 | C | T | 1 | a0003c0023t0001g0083 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.239+766C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474654 | |||||||
chr4:153474846 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+958G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474846 | |||||||
chr4:153474947 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0005t0001g0038 others(4): Show |
7 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+1059G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474947 | |||||||
chr4:153474981 | C | G | 69 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(66): Show |
69 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(66): Show |
intron_variant | MODIFIER | c.239+1093C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474981 | |||||||
chr4:153474990 | A | AC | 13 | a0001c0001t0001g0013 a0001c0002t0001g0024 a0001c0005t0001g0011 others(10): Show |
13 | HG01255.hp1 HG01891.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.239+1107dupC | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153474990 | ||||||
chr4:153474990 | A | AT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.239+1102_239+1103i others(3): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153474990 | |||||||
chr4:153475234 | G | A | 1 | a0001c0002t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.239+1346G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153475234 | |||||||
chr4:153475360 | C | T | 5 | a0001c0001t0001g0025 a0001c0002t0001g0017 a0001c0002t0001g0019 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+1472C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153475360 | |||||||
chr4:153475410 | C | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1522C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153475410 | |||||||
chr4:153475414 | C | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(23): Show |
26 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.239+1526C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153475414 | |||||||
chr4:153475682 | GA | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(23): Show |
26 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.239+1803delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153475682 | ||||||
chr4:153475728 | A | G | 11 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0097 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+1840A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153475728 | |||||||
chr4:153475759 | A | G | 1 | a0001c0024t0001g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239+1871A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153475759 | |||||||
chr4:153475795 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
48 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.239+1907C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153475795 | |||||||
chr4:153475962 | C | T | 1 | a0001c0020t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.239+2074C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153475962 | |||||||
chr4:153476270 | C | G | 2 | a0001c0001t0002g0082 a0001c0002t0002g0081 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.239+2382C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476270 | |||||||
chr4:153476385 | A | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+2497A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476385 | |||||||
chr4:153476394 | T | G | 1 | a0001c0003t0001g0167 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.239+2506T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476394 | |||||||
chr4:153476423 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.239+2535C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476423 | |||||||
chr4:153476561 | G | T | 1 | a0001c0022t0001g0114 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.239+2673G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476561 | |||||||
chr4:153476586 | A | C | 4 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+2698A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476586 | |||||||
chr4:153476720 | A | T | 1 | a0004c0018t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.239+2832A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476720 | |||||||
chr4:153476787 | T | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(23): Show |
26 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.239+2899T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476787 | |||||||
chr4:153476989 | T | A | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+3101T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476989 | |||||||
chr4:153476999 | T | C | 3 | a0001c0005t0001g0106 a0001c0028t0001g0108 a0003c0023t0001g0107 |
3 | HG01884.hp2 HG02148.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.239+3111T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153476999 | |||||||
chr4:153477445 | C | T | 85 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
85 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.239+3557C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477445 | |||||||
chr4:153477450 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0034t0001g0020 others(1): Show |
4 | HG03225.hp2 HG06807.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+3562C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477450 | |||||||
chr4:153477468 | T | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
28 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.239+3580T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477468 | |||||||
chr4:153477544 | G | A | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+3656G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477544 | |||||||
chr4:153477599 | TA | T | 8 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0004t0001g0152 others(5): Show |
8 | HG01928.hp1 HG01928.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+3721delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153477599 | ||||||
chr4:153477655 | G | A | 1 | a0004c0018t0001g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.239+3767G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477655 | |||||||
chr4:153477690 | A | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0042 others(49): Show |
52 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.239+3802A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477690 | |||||||
chr4:153477754 | A | G | 3 | a0001c0001t0001g0086 a0001c0005t0003g0034 a0014c0042t0001g0001 |
3 | HG03225.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+3866A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477754 | |||||||
chr4:153477781 | C | G | 8 | a0001c0002t0001g0113 a0001c0005t0001g0109 a0001c0005t0001g0111 others(5): Show |
8 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+3893C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477781 | |||||||
chr4:153477831 | C | T | 2 | a0001c0001t0001g0025 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239+3943C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477831 | |||||||
chr4:153477863 | A | G | 1 | a0001c0002t0001g0113 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.239+3975A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153477863 | |||||||
chr4:153478046 | A | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+4158A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153478046 | |||||||
chr4:153478110 | CTT | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+4223_239+4224d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153478110 | |||||||
chr4:153478540 | A | T | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+4652A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153478540 | |||||||
chr4:153478863 | A | G | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+4975A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153478863 | |||||||
chr4:153478890 | CTTAAAG | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0025 others(32): Show |
35 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.239+5007_239+5012d others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153478890 | ||||||
chr4:153478924 | C | T | 1 | a0010c0038t0001g0056 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.239+5036C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153478924 | |||||||
chr4:153479176 | C | T | 2 | a0011c0035t0001g0035 a0012c0032t0001g0036 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.239+5288C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153479176 | |||||||
chr4:153479863 | T | C | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+5975T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153479863 | |||||||
chr4:153480040 | A | G | 3 | a0001c0005t0001g0106 a0001c0028t0001g0108 a0003c0023t0001g0107 |
3 | HG01884.hp2 HG02148.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.239+6152A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480040 | |||||||
chr4:153480135 | C | T | 7 | a0001c0003t0001g0161 a0001c0003t0001g0163 a0001c0012t0001g0162 others(4): Show |
7 | HG00408.hp2 NA18952.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+6247C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480135 | |||||||
chr4:153480211 | C | T | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+6323C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480211 | |||||||
chr4:153480238 | C | T | 1 | a0001c0005t0001g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.239+6350C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480238 | |||||||
chr4:153480263 | C | T | 8 | a0001c0001t0001g0025 a0001c0005t0001g0106 a0001c0005t0001g0247 others(5): Show |
8 | HG01884.hp2 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+6375C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480263 | |||||||
chr4:153480293 | C | T | 3 | a0001c0012t0001g0205 a0002c0006t0001g0202 a0002c0006t0001g0203 |
3 | HG01496.hp2 HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.239+6405C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480293 | |||||||
chr4:153480377 | G | A | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+6489G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480377 | |||||||
chr4:153480430 | G | A | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+6542G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480430 | |||||||
chr4:153480502 | G | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
146 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.239+6614G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480502 | |||||||
chr4:153480517 | C | CA | 94 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(91): Show |
94 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.239+6651dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153480517 | ||||||
chr4:153480517 | C | CAA | 13 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(10): Show |
13 | HG02257.hp1 HG02647.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.239+6650_239+6651d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153480517 | ||||||
chr4:153480517 | CA | C | 10 | a0001c0003t0001g0201 a0001c0012t0001g0149 a0001c0014t0001g0150 others(7): Show |
10 | HG00408.hp1 HG01928.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.239+6651delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153480517 | ||||||
chr4:153480632 | C | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.239+6744C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480632 | |||||||
chr4:153480720 | T | G | 1 | a0002c0006t0001g0130 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.239+6832T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480720 | |||||||
chr4:153480785 | A | G | 9 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0245 others(6): Show |
9 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.239+6897A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480785 | |||||||
chr4:153480808 | T | C | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+6920T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480808 | |||||||
chr4:153480833 | A | G | 4 | a0001c0004t0001g0146 a0001c0004t0001g0147 a0001c0004t0001g0148 others(1): Show |
4 | NA18955.hp2 NA18960.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+6945A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480833 | |||||||
chr4:153480870 | C | T | 2 | a0001c0001t0002g0066 a0001c0002t0002g0065 |
2 | HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.239+6982C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153480870 | |||||||
chr4:153481045 | A | G | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+7157A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481045 | |||||||
chr4:153481166 | TTTCTC | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+7282_239+7286d others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153481166 | ||||||
chr4:153481219 | T | C | 1 | a0001c0002t0001g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.239+7331T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481219 | |||||||
chr4:153481346 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0002t0001g0002 others(12): Show |
15 | HG01255.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.239+7458G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481346 | |||||||
chr4:153481363 | G | A | 3 | a0001c0001t0001g0219 a0001c0002t0001g0245 a0001c0002t0001g0246 |
3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.239+7475G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481363 | |||||||
chr4:153481399 | A | C | 2 | a0002c0010t0001g0028 a0004c0018t0001g0029 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.239+7511A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481399 | |||||||
chr4:153481648 | A | G | 1 | a0002c0010t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.239+7760A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481648 | |||||||
chr4:153481683 | C | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0042 others(49): Show |
52 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.239+7795C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481683 | |||||||
chr4:153481700 | T | A | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+7812T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481700 | |||||||
chr4:153481744 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0223 others(22): Show |
25 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.239+7856C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481744 | |||||||
chr4:153481826 | C | G | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.239+7938C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481826 | |||||||
chr4:153481909 | C | T | 1 | a0001c0011t0001g0079 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.239+8021C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153481909 | |||||||
chr4:153482097 | G | C | 1 | a0001c0005t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.239+8209G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482097 | |||||||
chr4:153482100 | T | C | 1 | a0001c0005t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.239+8212T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482100 | |||||||
chr4:153482192 | A | G | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+8304A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482192 | |||||||
chr4:153482323 | A | AT | 75 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0039 others(72): Show |
75 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.239+8442dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153482323 | ||||||
chr4:153482391 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+8503G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482391 | |||||||
chr4:153482441 | T | A | 1 | a0001c0012t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.239+8553T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482441 | |||||||
chr4:153482451 | A | C | 2 | a0001c0001t0001g0042 a0002c0031t0001g0043 |
2 | NA18986.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.239+8563A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482451 | |||||||
chr4:153482741 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0013t0001g0044 others(1): Show |
4 | HG00597.hp1 NA18986.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+8853G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482741 | |||||||
chr4:153482870 | C | T | 3 | a0001c0014t0001g0155 a0003c0019t0001g0153 a0003c0019t0001g0154 |
3 | HG01928.hp2 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.239+8982C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482870 | |||||||
chr4:153482886 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.239+8998C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482886 | |||||||
chr4:153482949 | A | G | 8 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(5): Show |
8 | HG02257.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+9061A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482949 | |||||||
chr4:153482954 | C | T | 7 | a0001c0001t0001g0227 a0001c0002t0001g0017 a0001c0002t0001g0019 others(4): Show |
7 | HG02559.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+9066C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482954 | |||||||
chr4:153482975 | A | T | 7 | a0001c0001t0001g0227 a0001c0002t0001g0017 a0001c0002t0001g0019 others(4): Show |
7 | HG02559.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+9087A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153482975 | |||||||
chr4:153483036 | A | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+9148A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153483036 | |||||||
chr4:153483190 | C | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+9302C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153483190 | |||||||
chr4:153483420 | GGCTGGGT others(19): Show |
G | 4 | a0001c0005t0001g0247 a0004c0027t0001g0248 a0011c0035t0001g0035 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+9535_239+9560d others(28): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153483420 | ||||||
chr4:153483953 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239+10065G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153483953 | |||||||
chr4:153484010 | C | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+10122C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484010 | |||||||
chr4:153484152 | G | A | 2 | a0001c0003t0001g0206 a0006c0050t0001g0116 |
2 | HG02300.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.239+10264G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484152 | |||||||
chr4:153484468 | T | G | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+10580T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484468 | |||||||
chr4:153484476 | A | T | 1 | a0001c0004t0001g0115 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.239+10588A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484476 | |||||||
chr4:153484531 | C | T | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+10643C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484531 | |||||||
chr4:153484561 | C | T | 9 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0245 others(6): Show |
9 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.239+10673C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484561 | |||||||
chr4:153484625 | C | T | 2 | a0001c0001t0001g0025 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239+10737C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484625 | |||||||
chr4:153484627 | C | G | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+10739C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484627 | |||||||
chr4:153484703 | T | C | 1 | a0001c0008t0001g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.239+10815T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484703 | |||||||
chr4:153484715 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+10827G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484715 | |||||||
chr4:153484737 | A | G | 147 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(144): Show |
147 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.239+10849A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484737 | |||||||
chr4:153484987 | C | T | 3 | a0001c0001t0001g0086 a0001c0005t0003g0034 a0014c0042t0001g0001 |
3 | HG03225.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+11099C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153484987 | |||||||
chr4:153485067 | C | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.239+11179C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153485067 | |||||||
chr4:153485121 | T | TA | 24 | a0001c0001t0001g0041 a0001c0001t0001g0095 a0001c0001t0001g0233 others(21): Show |
24 | HG00597.hp1 HG01109.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.239+11257dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153485121 | ||||||
chr4:153485121 | TA | T | 15 | a0001c0001t0001g0025 a0001c0001t0001g0227 a0001c0002t0001g0017 others(12): Show |
15 | HG00609.hp1 HG01346.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.239+11257delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153485121 | ||||||
chr4:153485121 | TAA | T | 35 | a0001c0003t0001g0122 a0001c0003t0001g0141 a0001c0004t0001g0115 others(32): Show |
35 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.239+11256_239+1125 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153485121 | ||||||
chr4:153485173 | A | G | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+11285A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153485173 | |||||||
chr4:153485213 | C | G | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+11325C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153485213 | |||||||
chr4:153485526 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(155): Show |
158 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.239+11638A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153485526 | |||||||
chr4:153485642 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(155): Show |
158 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.239+11754A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153485642 | |||||||
chr4:153486082 | C | T | 3 | a0001c0002t0001g0054 a0001c0002t0001g0057 a0001c0005t0001g0055 |
3 | HG02071.hp1 NA18991.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.239+12194C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486082 | |||||||
chr4:153486142 | A | G | 1 | a0001c0003t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.239+12254A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486142 | |||||||
chr4:153486155 | A | G | 11 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0002t0001g0051 others(8): Show |
11 | HG00597.hp1 HG02071.hp1 NA18972.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+12267A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486155 | |||||||
chr4:153486173 | C | T | 4 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+12285C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486173 | |||||||
chr4:153486270 | C | T | 1 | a0002c0006t0001g0200 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.239+12382C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486270 | |||||||
chr4:153486531 | A | T | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+12643A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486531 | |||||||
chr4:153486682 | G | A | 39 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(36): Show |
39 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.239+12794G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486682 | |||||||
chr4:153486702 | A | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+12814A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486702 | |||||||
chr4:153486844 | A | G | 4 | a0001c0001t0001g0008 a0001c0021t0001g0014 a0001c0024t0001g0010 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+12956A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486844 | |||||||
chr4:153486847 | C | T | 2 | a0002c0010t0001g0028 a0004c0018t0001g0029 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.239+12959C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486847 | |||||||
chr4:153486942 | C | T | 6 | a0001c0002t0001g0100 a0001c0005t0001g0247 a0001c0033t0001g0099 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+13054C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153486942 | |||||||
chr4:153487024 | T | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.239+13136T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487024 | |||||||
chr4:153487127 | C | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(158): Show |
161 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.239+13239C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487127 | |||||||
chr4:153487208 | A | C | 106 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(103): Show |
106 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.239+13320A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487208 | |||||||
chr4:153487302 | A | G | 59 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(56): Show |
59 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.239+13414A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487302 | |||||||
chr4:153487326 | C | T | 1 | a0001c0005t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.239+13438C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487326 | |||||||
chr4:153487394 | A | G | 1 | a0001c0022t0001g0078 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.239+13506A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487394 | |||||||
chr4:153487459 | C | G | 1 | a0001c0008t0001g0199 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.239+13571C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487459 | |||||||
chr4:153487480 | G | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 others(1): Show |
4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+13592G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487480 | |||||||
chr4:153487693 | C | CGT | 24 | a0001c0001t0001g0025 a0001c0001t0001g0223 a0001c0001t0001g0224 others(21): Show |
24 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.239+13831_239+1383 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487693 | ||||||
chr4:153487693 | C | CGTGT | 17 | a0001c0001t0001g0089 a0001c0001t0001g0226 a0001c0001t0001g0233 others(14): Show |
17 | HG01496.hp2 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.239+13829_239+1383 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487693 | ||||||
chr4:153487693 | C | CGTGTGT | 41 | a0001c0001t0001g0086 a0001c0002t0001g0113 a0001c0003t0001g0122 others(38): Show |
41 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.239+13827_239+1383 others(10): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487693 | ||||||
chr4:153487693 | C | CGTGTGTG others(1): Show |
17 | a0001c0003t0001g0133 a0001c0003t0001g0141 a0001c0004t0001g0115 others(14): Show |
17 | HG00558.hp1 HG01109.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.239+13825_239+1383 others(12): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487693 | ||||||
chr4:153487693 | C | CGTGTGTG others(3): Show |
4 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0014t0001g0144 others(1): Show |
4 | HG01243.hp2 HG02300.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+13823_239+1383 others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487693 | ||||||
chr4:153487719 | T | TGA | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0100 others(2): Show |
5 | HG02145.hp1 HG03017.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+13850_239+1385 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487719 | ||||||
chr4:153487719 | T | TGTGTGA | 41 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(38): Show |
41 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.239+13832_239+1383 others(10): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487719 | ||||||
chr4:153487719 | T | TGTGTGTG others(1): Show |
11 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0066 others(8): Show |
11 | HG02257.hp1 HG02523.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+13832_239+1383 others(12): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487719 | ||||||
chr4:153487719 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0002g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.239+13832_239+1383 others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487719 | ||||||
chr4:153487719 | TGAGA | T | 3 | a0001c0005t0001g0106 a0001c0028t0001g0108 a0003c0023t0001g0107 |
3 | HG01884.hp2 HG02148.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.239+13848_239+1385 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153487719 | ||||||
chr4:153487721 | A | T | 53 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(50): Show |
53 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.239+13833A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487721 | |||||||
chr4:153487723 | A | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.239+13835A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487723 | |||||||
chr4:153487810 | A | G | 1 | a0001c0004t0001g0214 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.239+13922A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487810 | |||||||
chr4:153487812 | G | C | 1 | a0001c0004t0001g0214 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.239+13924G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153487812 | |||||||
chr4:153488000 | T | TGAGA | 245 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.239+14115_239+1411 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153488000 | ||||||
chr4:153488039 | G | GGT | 8 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0245 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+14162_239+1416 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153488039 | ||||||
chr4:153488121 | G | C | 1 | a0001c0004t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.239+14233G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488121 | |||||||
chr4:153488162 | TGAGA | T | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+14283_239+1428 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153488162 | ||||||
chr4:153488253 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.239+14365G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488253 | |||||||
chr4:153488411 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.239+14523G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488411 | |||||||
chr4:153488422 | G | C | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+14534G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488422 | |||||||
chr4:153488537 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.239+14649G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488537 | |||||||
chr4:153488757 | G | A | 5 | a0001c0001t0001g0039 a0001c0002t0001g0009 a0001c0005t0001g0038 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+14869G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488757 | |||||||
chr4:153488793 | C | T | 2 | a0001c0003t0001g0122 a0001c0012t0001g0126 |
2 | HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.239+14905C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488793 | |||||||
chr4:153488803 | G | C | 39 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(36): Show |
39 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.239+14915G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488803 | |||||||
chr4:153488897 | G | T | 6 | a0001c0002t0001g0100 a0001c0005t0001g0247 a0001c0033t0001g0099 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+15009G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488897 | |||||||
chr4:153488984 | C | G | 43 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0003t0001g0122 others(40): Show |
43 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.239+15096C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153488984 | |||||||
chr4:153489283 | G | C | 2 | a0001c0003t0001g0181 a0001c0003t0001g0201 |
2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.239+15395G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153489283 | |||||||
chr4:153489418 | G | A | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+15530G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153489418 | |||||||
chr4:153489458 | A | C | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+15570A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153489458 | |||||||
chr4:153489538 | T | C | 55 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0227 others(52): Show |
55 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.239+15650T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153489538 | |||||||
chr4:153489681 | T | G | 1 | a0001c0012t0001g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.239+15793T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153489681 | |||||||
chr4:153489715 | G | A | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+15827G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153489715 | |||||||
chr4:153489787 | T | C | 1 | a0001c0008t0001g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.239+15899T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153489787 | |||||||
chr4:153489804 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.239+15916A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153489804 | |||||||
chr4:153490087 | T | G | 4 | a0001c0005t0001g0247 a0004c0027t0001g0248 a0011c0035t0001g0035 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+16199T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153490087 | |||||||
chr4:153490226 | C | T | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+16338C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153490226 | |||||||
chr4:153490245 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.239+16357G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153490245 | |||||||
chr4:153490392 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.239+16504G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153490392 | |||||||
chr4:153490411 | G | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(174): Show |
177 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.239+16523G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153490411 | |||||||
chr4:153490726 | C | T | 2 | a0002c0010t0001g0028 a0004c0018t0001g0029 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.239+16838C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153490726 | |||||||
chr4:153490808 | G | A | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+16920G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153490808 | |||||||
chr4:153490922 | C | T | 1 | a0002c0045t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.239+17034C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153490922 | |||||||
chr4:153490953 | C | CA | 11 | a0001c0003t0001g0167 a0001c0003t0001g0182 a0001c0003t0001g0183 others(8): Show |
11 | HG00140.hp2 HG01361.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+17086dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153490953 | ||||||
chr4:153490953 | CA | C | 63 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0042 others(60): Show |
63 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.239+17086delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153490953 | ||||||
chr4:153490953 | CAA | C | 47 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0100 others(44): Show |
47 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.239+17085_239+1708 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153490953 | ||||||
chr4:153491233 | C | T | 4 | a0001c0004t0001g0212 a0001c0014t0001g0211 a0002c0006t0001g0132 others(1): Show |
4 | HG00609.hp1 HG02135.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+17345C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153491233 | |||||||
chr4:153491242 | C | T | 2 | a0001c0003t0001g0196 a0002c0016t0001g0215 |
2 | HG00735.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.239+17354C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153491242 | |||||||
chr4:153491243 | T | C | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+17355T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153491243 | |||||||
chr4:153491400 | C | T | 43 | a0001c0001t0001g0227 a0001c0002t0001g0024 a0001c0003t0001g0122 others(40): Show |
43 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.239+17512C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153491400 | |||||||
chr4:153492044 | G | A | 1 | a0001c0008t0001g0199 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.239+18156G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492044 | |||||||
chr4:153492072 | G | T | 1 | a0010c0038t0001g0056 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.239+18184G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492072 | |||||||
chr4:153492082 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(160): Show |
163 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.239+18194A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492082 | |||||||
chr4:153492104 | C | T | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+18216C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492104 | |||||||
chr4:153492172 | TA | T | 59 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(56): Show |
59 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.239+18297delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153492172 | ||||||
chr4:153492174 | A | T | 1 | a0008c0052t0001g0120 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.239+18286A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492174 | |||||||
chr4:153492290 | C | T | 5 | a0001c0005t0001g0022 a0001c0059t0001g0033 a0002c0010t0001g0021 others(2): Show |
5 | HG02922.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+18402C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492290 | |||||||
chr4:153492317 | T | A | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.239+18429T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492317 | |||||||
chr4:153492762 | TG | T | 58 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(55): Show |
58 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.239+18875delG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492762 | |||||||
chr4:153492809 | C | A | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+18921C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492809 | |||||||
chr4:153492896 | C | T | 41 | a0001c0001t0001g0227 a0001c0003t0001g0122 a0001c0003t0001g0133 others(38): Show |
41 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.239+19008C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153492896 | |||||||
chr4:153493036 | G | C | 2 | a0001c0008t0001g0176 a0001c0008t0001g0184 |
2 | HG01071.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.239+19148G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493036 | |||||||
chr4:153493112 | C | T | 4 | a0001c0001t0001g0008 a0001c0021t0001g0014 a0001c0024t0001g0010 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+19224C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493112 | |||||||
chr4:153493118 | A | G | 58 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0227 others(55): Show |
58 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.239+19230A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493118 | |||||||
chr4:153493237 | T | C | 1 | a0001c0012t0001g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.239+19349T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493237 | |||||||
chr4:153493345 | C | CAAAAAAA others(3): Show |
1 | a0001c0005t0003g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.239+19470_239+1947 others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153493345 | ||||||
chr4:153493345 | C | CAAAAAAA others(11): Show |
4 | a0001c0005t0001g0022 a0001c0059t0001g0033 a0002c0010t0001g0021 others(1): Show |
4 | HG02922.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+19462_239+1947 others(22): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153493345 | ||||||
chr4:153493345 | C | CAAAAAAA others(12): Show |
1 | a0013c0058t0001g0031 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.239+19461_239+1947 others(23): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153493345 | ||||||
chr4:153493345 | C | CAAAAAAA others(15): Show |
2 | a0001c0005t0001g0247 a0004c0027t0001g0248 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.239+19458_239+1947 others(26): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153493345 | ||||||
chr4:153493345 | C | CAAAAAAA others(19): Show |
2 | a0011c0035t0001g0035 a0012c0032t0001g0036 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.239+19479_239+1948 others(30): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153493345 | ||||||
chr4:153493345 | CAA | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0004t0001g0125 others(7): Show |
10 | HG00140.hp1 HG00558.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.239+19478_239+1947 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153493345 | ||||||
chr4:153493345 | CAAA | C | 91 | a0001c0001t0001g0041 a0001c0001t0001g0058 a0001c0001t0001g0059 others(88): Show |
91 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.239+19477_239+1947 others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153493345 | ||||||
chr4:153493517 | G | T | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+19629G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493517 | |||||||
chr4:153493523 | G | A | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+19635G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493523 | |||||||
chr4:153493530 | C | T | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+19642C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493530 | |||||||
chr4:153493689 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.239+19801C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493689 | |||||||
chr4:153493690 | G | A | 2 | a0002c0006t0001g0118 a0008c0052t0001g0120 |
2 | NA18943.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.239+19802G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493690 | |||||||
chr4:153493772 | C | T | 41 | a0001c0001t0001g0227 a0001c0003t0001g0122 a0001c0003t0001g0133 others(38): Show |
41 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.239+19884C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153493772 | |||||||
chr4:153494000 | A | G | 2 | a0001c0001t0001g0025 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239+20112A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494000 | |||||||
chr4:153494032 | T | C | 125 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0041 others(122): Show |
125 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.239+20144T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494032 | |||||||
chr4:153494118 | A | T | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+20230A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494118 | |||||||
chr4:153494120 | A | C | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+20232A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494120 | |||||||
chr4:153494213 | G | A | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.239+20325G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494213 | |||||||
chr4:153494230 | C | T | 2 | a0005c0017t0001g0026 a0005c0017t0001g0027 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.239+20342C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494230 | |||||||
chr4:153494513 | G | T | 2 | a0001c0001t0001g0025 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239+20625G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494513 | |||||||
chr4:153494626 | C | T | 6 | a0001c0005t0001g0022 a0001c0059t0001g0033 a0002c0010t0001g0021 others(3): Show |
6 | HG02615.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.239+20738C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494626 | |||||||
chr4:153494867 | T | A | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.239+20979T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494867 | |||||||
chr4:153494879 | C | G | 9 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0100 others(6): Show |
9 | HG02145.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.239+20991C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494879 | |||||||
chr4:153494980 | C | G | 78 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0042 others(75): Show |
78 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.239+21092C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153494980 | |||||||
chr4:153495099 | G | A | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+21211G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153495099 | |||||||
chr4:153495141 | C | G | 1 | a0001c0003t0001g0122 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.239+21253C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153495141 | |||||||
chr4:153495226 | A | G | 2 | a0001c0002t0001g0007 a0001c0002t0002g0080 |
2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.239+21338A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153495226 | |||||||
chr4:153495248 | C | T | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+21360C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153495248 | |||||||
chr4:153495266 | C | G | 58 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(55): Show |
58 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.239+21378C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153495266 | |||||||
chr4:153495329 | A | C | 67 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.239+21441A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153495329 | |||||||
chr4:153495357 | A | G | 2 | a0001c0005t0001g0022 a0002c0010t0001g0021 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.239+21469A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153495357 | |||||||
chr4:153495895 | A | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.239+22007A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153495895 | |||||||
chr4:153496035 | A | G | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.239+22147A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153496035 | |||||||
chr4:153496327 | G | T | 4 | a0001c0005t0001g0247 a0004c0027t0001g0248 a0011c0035t0001g0035 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+22439G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153496327 | |||||||
chr4:153496355 | G | A | 2 | a0001c0001t0001g0025 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239+22467G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153496355 | |||||||
chr4:153496823 | A | G | 1 | a0001c0005t0001g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.239+22935A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153496823 | |||||||
chr4:153496867 | T | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0086 others(17): Show |
20 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.239+22979T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153496867 | |||||||
chr4:153496962 | G | C | 5 | a0001c0005t0001g0106 a0001c0028t0001g0108 a0002c0010t0001g0028 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+23074G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153496962 | |||||||
chr4:153497035 | G | GT | 4 | a0001c0001t0001g0025 a0001c0011t0001g0050 a0001c0034t0001g0020 others(1): Show |
4 | NA18906.hp2 NA18978.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+23154dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153497035 | ||||||
chr4:153497409 | T | C | 72 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(69): Show |
72 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.239+23521T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153497409 | |||||||
chr4:153497716 | C | T | 4 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 others(1): Show |
4 | HG01243.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+23828C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153497716 | |||||||
chr4:153497802 | T | C | 100 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(97): Show |
100 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.239+23914T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153497802 | |||||||
chr4:153497848 | CT | C | 9 | a0001c0004t0001g0135 a0001c0005t0001g0022 a0001c0005t0001g0247 others(6): Show |
9 | HG02615.hp2 HG02886.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+23968delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153497848 | ||||||
chr4:153497878 | C | CA | 5 | a0001c0003t0001g0181 a0001c0005t0001g0055 a0001c0011t0001g0050 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+24011dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153497878 | ||||||
chr4:153497878 | C | CAA | 5 | a0001c0001t0001g0086 a0001c0001t0001g0227 a0001c0005t0003g0034 others(2): Show |
5 | HG02559.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+24010_239+2401 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153497878 | ||||||
chr4:153497878 | CA | C | 57 | a0001c0001t0001g0041 a0001c0001t0001g0224 a0001c0001t0001g0225 others(54): Show |
57 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.239+24011delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153497878 | ||||||
chr4:153497878 | CAA | C | 9 | a0001c0001t0002g0066 a0001c0002t0001g0017 a0001c0002t0001g0019 others(6): Show |
9 | HG02004.hp1 HG02895.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.239+24010_239+2401 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153497878 | ||||||
chr4:153497878 | CAAAAAAA | C | 6 | a0001c0004t0001g0137 a0001c0004t0001g0146 a0001c0004t0001g0147 others(3): Show |
6 | NA18953.hp1 NA18955.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+24005_239+2401 others(11): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153497878 | ||||||
chr4:153497878 | CAAAAAAA others(5): Show |
C | 3 | a0002c0006t0001g0164 a0002c0006t0001g0165 a0002c0025t0001g0166 |
3 | NA18952.hp2 NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.239+24000_239+2401 others(16): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153497878 | ||||||
chr4:153497880 | A | G | 5 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+23992A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153497880 | |||||||
chr4:153497893 | A | G | 1 | a0001c0013t0001g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.239+24005A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153497893 | |||||||
chr4:153497895 | A | G | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.239+24007A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153497895 | |||||||
chr4:153497924 | G | A | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(4): Show |
7 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+24036G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153497924 | |||||||
chr4:153498036 | C | T | 10 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0005t0001g0022 others(7): Show |
10 | HG02615.hp2 HG02886.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.239+24148C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498036 | |||||||
chr4:153498070 | G | A | 8 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0003t0001g0119 others(5): Show |
8 | HG02004.hp1 HG03017.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+24182G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498070 | |||||||
chr4:153498180 | T | C | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+24292T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498180 | |||||||
chr4:153498304 | C | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(76): Show |
79 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.239+24416C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498304 | |||||||
chr4:153498315 | A | G | 1 | a0002c0015t0001g0018 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.239+24427A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498315 | |||||||
chr4:153498349 | G | C | 10 | a0001c0003t0001g0157 a0001c0003t0001g0163 a0001c0003t0001g0239 others(7): Show |
10 | HG00544.hp2 HG00597.hp2 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.239+24461G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498349 | |||||||
chr4:153498356 | G | A | 1 | a0001c0024t0001g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239+24468G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498356 | |||||||
chr4:153498419 | T | A | 53 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(50): Show |
53 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.239+24531T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498419 | |||||||
chr4:153498559 | G | A | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+24671G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498559 | |||||||
chr4:153498609 | A | G | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.239+24721A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498609 | |||||||
chr4:153498686 | C | T | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+24798C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153498686 | |||||||
chr4:153499165 | C | T | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+25277C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499165 | |||||||
chr4:153499173 | G | A | 15 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0017 others(12): Show |
15 | HG01243.hp2 HG02004.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.239+25285G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499173 | |||||||
chr4:153499188 | C | T | 2 | a0001c0001t0001g0025 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239+25300C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499188 | |||||||
chr4:153499346 | G | C | 2 | a0001c0002t0001g0007 a0001c0002t0002g0080 |
2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.239+25458G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499346 | |||||||
chr4:153499429 | AT | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(98): Show |
101 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.239+25558delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153499429 | ||||||
chr4:153499453 | C | T | 1 | a0001c0024t0001g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239+25565C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499453 | |||||||
chr4:153499454 | G | A | 8 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0003t0001g0119 others(5): Show |
8 | HG02004.hp1 HG03017.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+25566G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499454 | |||||||
chr4:153499576 | G | C | 8 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0003t0001g0119 others(5): Show |
8 | HG02004.hp1 HG03017.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+25688G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499576 | |||||||
chr4:153499588 | G | A | 15 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0017 others(12): Show |
15 | HG01243.hp2 HG02004.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.239+25700G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499588 | |||||||
chr4:153499838 | G | T | 17 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0017 others(14): Show |
17 | HG01243.hp2 HG02004.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.239+25950G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499838 | |||||||
chr4:153499886 | G | A | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.239+25998G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499886 | |||||||
chr4:153499914 | C | G | 17 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0017 others(14): Show |
17 | HG01243.hp2 HG02004.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.239+26026C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499914 | |||||||
chr4:153499932 | T | C | 4 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+26044T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153499932 | |||||||
chr4:153499952 | A | AT | 14 | a0001c0001t0001g0227 a0001c0002t0001g0002 a0001c0002t0001g0005 others(11): Show |
14 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.239+26075dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153499952 | ||||||
chr4:153500025 | G | A | 1 | a0001c0026t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.239+26137G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500025 | |||||||
chr4:153500031 | ACCTT | A | 15 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0017 others(12): Show |
15 | HG01243.hp2 HG02004.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.239+26151_239+2615 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153500031 | ||||||
chr4:153500035 | T | TCCTC | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+26150_239+2615 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153500035 | ||||||
chr4:153500039 | T | C | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+26151T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500039 | |||||||
chr4:153500043 | C | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
75 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.239+26155C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500043 | |||||||
chr4:153500043 | C | T | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+26155C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500043 | |||||||
chr4:153500047 | T | C | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+26159T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500047 | |||||||
chr4:153500049 | CTCCCTTC others(3): Show |
C | 1 | a0001c0004t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.239+26180_239+2618 others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153500049 | ||||||
chr4:153500053 | C | G | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+26165C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500053 | |||||||
chr4:153500058 | G | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+26170G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500058 | |||||||
chr4:153500058 | G | C | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+26170G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500058 | |||||||
chr4:153500068 | G | C | 20 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0227 others(17): Show |
20 | HG01243.hp2 HG02004.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.239+26180G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500068 | |||||||
chr4:153500157 | A | G | 17 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0017 others(14): Show |
17 | HG01243.hp2 HG02004.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.239+26269A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500157 | |||||||
chr4:153500223 | C | G | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+26335C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500223 | |||||||
chr4:153500282 | C | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(101): Show |
104 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.239+26394C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500282 | |||||||
chr4:153500287 | G | A | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+26399G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500287 | |||||||
chr4:153500322 | T | C | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+26434T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500322 | |||||||
chr4:153500376 | G | A | 10 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0245 others(7): Show |
10 | HG02004.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.239+26488G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500376 | |||||||
chr4:153500764 | A | G | 10 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0245 others(7): Show |
10 | HG02004.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.239+26876A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500764 | |||||||
chr4:153500796 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0005t0001g0038 others(4): Show |
7 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+26908C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500796 | |||||||
chr4:153500797 | G | A | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+26909G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500797 | |||||||
chr4:153500806 | C | T | 5 | a0001c0005t0001g0022 a0001c0024t0001g0015 a0002c0010t0001g0021 others(2): Show |
5 | HG02922.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+26918C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500806 | |||||||
chr4:153500826 | C | T | 1 | a0002c0007t0001g0084 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.239+26938C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153500826 | |||||||
chr4:153501066 | A | C | 1 | a0001c0002t0001g0213 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.239+27178A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501066 | |||||||
chr4:153501103 | G | A | 4 | a0001c0005t0001g0022 a0002c0010t0001g0021 a0002c0057t0001g0032 others(1): Show |
4 | HG02922.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+27215G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501103 | |||||||
chr4:153501132 | A | G | 1 | a0006c0040t0001g0030 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.239+27244A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501132 | |||||||
chr4:153501140 | C | T | 1 | a0001c0012t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.239+27252C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501140 | |||||||
chr4:153501202 | G | GT | 17 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0095 others(14): Show |
17 | HG00597.hp1 HG01192.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.239+27335dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153501202 | ||||||
chr4:153501202 | GT | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0039 others(69): Show |
72 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.239+27335delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153501202 | ||||||
chr4:153501297 | G | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0013t0001g0044 others(1): Show |
4 | HG00597.hp1 NA18986.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+27409G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501297 | |||||||
chr4:153501310 | T | C | 1 | a0001c0014t0001g0211 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.239+27422T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501310 | |||||||
chr4:153501357 | C | T | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+27469C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501357 | |||||||
chr4:153501597 | ATTAC | A | 2 | a0001c0005t0001g0247 a0004c0027t0001g0248 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.239+27712_239+2771 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153501597 | ||||||
chr4:153501697 | A | G | 2 | a0001c0001t0001g0025 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239+27809A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501697 | |||||||
chr4:153501789 | A | G | 1 | a0001c0003t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239+27901A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501789 | |||||||
chr4:153501828 | T | A | 1 | a0004c0018t0001g0003 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.239+27940T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153501828 | |||||||
chr4:153501943 | G | GT | 23 | a0001c0001t0001g0041 a0001c0002t0001g0057 a0001c0002t0001g0245 others(20): Show |
23 | HG00597.hp1 HG01099.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.239+28078dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153501943 | ||||||
chr4:153501943 | G | GTTT | 74 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(71): Show |
74 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.239+28076_239+2807 others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153501943 | ||||||
chr4:153501943 | G | GTTTT | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0002t0001g0217 others(13): Show |
16 | HG01255.hp1 HG01361.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.239+28075_239+2807 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153501943 | ||||||
chr4:153502052 | A | G | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.239+28164A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153502052 | |||||||
chr4:153502140 | C | A | 1 | a0001c0004t0001g0152 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.239+28252C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153502140 | |||||||
chr4:153502157 | C | T | 8 | a0001c0005t0001g0022 a0001c0005t0001g0247 a0002c0010t0001g0021 others(5): Show |
8 | HG02615.hp2 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+28269C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153502157 | |||||||
chr4:153502464 | C | T | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+28576C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153502464 | |||||||
chr4:153502494 | G | A | 8 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0003t0001g0119 others(5): Show |
8 | HG02004.hp1 HG03017.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+28606G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153502494 | |||||||
chr4:153502521 | C | T | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+28633C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153502521 | |||||||
chr4:153502643 | C | G | 169 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(166): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.239+28755C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153502643 | |||||||
chr4:153502896 | A | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+29008A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153502896 | |||||||
chr4:153502973 | C | CT | 163 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(160): Show |
163 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.239+29095dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153502973 | ||||||
chr4:153503104 | A | G | 1 | a0001c0005t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239+29216A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153503104 | |||||||
chr4:153503315 | A | T | 3 | a0001c0003t0001g0172 a0001c0003t0001g0173 a0001c0009t0001g0175 |
3 | NA18978.hp1 NA18981.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.239+29427A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153503315 | |||||||
chr4:153503408 | A | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(91): Show |
94 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.239+29520A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153503408 | |||||||
chr4:153503665 | T | G | 3 | a0001c0012t0001g0205 a0002c0006t0001g0202 a0002c0006t0001g0203 |
3 | HG01496.hp2 HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.239+29777T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153503665 | |||||||
chr4:153503829 | C | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(85): Show |
88 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.239+29941C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153503829 | |||||||
chr4:153503908 | C | T | 1 | a0001c0008t0001g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.239+30020C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153503908 | |||||||
chr4:153503999 | C | T | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+30111C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153503999 | |||||||
chr4:153504016 | G | C | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+30128G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504016 | |||||||
chr4:153504091 | C | T | 5 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
5 | HG02622.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+30203C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504091 | |||||||
chr4:153504111 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(67): Show |
70 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.239+30223C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504111 | |||||||
chr4:153504266 | C | CT | 7 | a0001c0001t0001g0244 a0001c0005t0001g0055 a0001c0005t0001g0106 others(4): Show |
7 | HG02148.hp1 HG02970.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+30409dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | C | CTTTTTTT others(3): Show |
2 | a0001c0056t0001g0160 a0002c0006t0001g0118 |
2 | NA18991.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.239+30400_239+3040 others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CT | C | 58 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0002t0001g0047 others(55): Show |
58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.239+30409delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTT | C | 37 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0236 others(34): Show |
37 | HG00140.hp2 HG00544.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.239+30408_239+3040 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTT | C | 6 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0005t0003g0034 others(3): Show |
6 | HG01243.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+30406_239+3040 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTTT | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+30405_239+3040 others(9): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTTTT | C | 32 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0097 others(29): Show |
32 | HG01255.hp1 HG01891.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.239+30404_239+3040 others(10): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTTTTT | C | 7 | a0001c0005t0001g0022 a0001c0005t0001g0247 a0002c0010t0001g0021 others(4): Show |
7 | HG02886.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+30403_239+3040 others(11): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0227 a0002c0007t0001g0229 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.239+30397_239+3040 others(17): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTTTTT others(7): Show |
C | 2 | a0001c0009t0001g0158 a0002c0007t0001g0228 |
2 | HG00597.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.239+30396_239+3040 others(18): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTTTTT others(8): Show |
C | 1 | a0001c0004t0001g0134 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.239+30395_239+3040 others(19): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTTTTT others(9): Show |
C | 37 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(34): Show |
37 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.239+30394_239+3040 others(20): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504266 | CTTTTTTT others(12): Show |
C | 1 | a0001c0002t0001g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.239+30391_239+3040 others(23): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153504266 | ||||||
chr4:153504335 | A | G | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+30447A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504335 | |||||||
chr4:153504349 | G | A | 3 | a0001c0005t0001g0106 a0001c0028t0001g0108 a0003c0023t0001g0107 |
3 | HG01884.hp2 HG02148.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.239+30461G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504349 | |||||||
chr4:153504426 | C | T | 8 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(5): Show |
8 | HG02257.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+30538C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504426 | |||||||
chr4:153504427 | G | A | 8 | a0001c0002t0001g0113 a0001c0005t0001g0109 a0001c0005t0001g0111 others(5): Show |
8 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.239+30539G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504427 | |||||||
chr4:153504436 | C | T | 84 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(81): Show |
84 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.239+30548C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504436 | |||||||
chr4:153504579 | T | C | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+30691T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504579 | |||||||
chr4:153504581 | T | G | 1 | a0002c0007t0001g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.239+30693T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504581 | |||||||
chr4:153504699 | A | G | 9 | a0001c0001t0001g0025 a0001c0005t0001g0022 a0001c0005t0001g0247 others(6): Show |
9 | HG02886.hp2 HG02922.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.239+30811A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504699 | |||||||
chr4:153504762 | A | G | 5 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+30874A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504762 | |||||||
chr4:153504924 | G | A | 1 | a0004c0018t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.239+31036G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153504924 | |||||||
chr4:153505109 | C | CT | 12 | a0001c0001t0001g0041 a0001c0002t0001g0100 a0001c0002t0001g0113 others(9): Show |
12 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.239+31236dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153505109 | ||||||
chr4:153505109 | C | CTT | 8 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0005t0001g0038 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+31235_239+3123 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153505109 | ||||||
chr4:153505109 | CTT | C | 8 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0003t0001g0119 others(5): Show |
8 | HG02004.hp1 HG03017.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+31235_239+3123 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153505109 | ||||||
chr4:153505146 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.239+31258G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505146 | |||||||
chr4:153505187 | A | G | 2 | a0001c0001t0001g0089 a0001c0002t0001g0092 |
2 | NA18944.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.239+31299A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505187 | |||||||
chr4:153505199 | C | T | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+31311C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505199 | |||||||
chr4:153505203 | T | C | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+31315T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505203 | |||||||
chr4:153505259 | A | G | 10 | a0001c0002t0001g0213 a0001c0003t0001g0117 a0001c0003t0001g0172 others(7): Show |
10 | HG00544.hp1 HG00609.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.239+31371A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505259 | |||||||
chr4:153505338 | C | T | 5 | a0001c0014t0001g0150 a0001c0014t0001g0155 a0002c0015t0001g0151 others(2): Show |
5 | HG01928.hp2 HG01993.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+31450C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505338 | |||||||
chr4:153505341 | C | T | 8 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0003t0001g0119 others(5): Show |
8 | HG02004.hp1 HG03017.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+31453C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505341 | |||||||
chr4:153505359 | A | G | 2 | a0001c0001t0001g0025 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239+31471A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505359 | |||||||
chr4:153505390 | G | A | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239+31502G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505390 | |||||||
chr4:153505427 | G | A | 198 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(195): Show |
198 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.239+31539G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505427 | |||||||
chr4:153505525 | A | G | 1 | a0001c0013t0001g0087 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.239+31637A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505525 | |||||||
chr4:153505578 | C | T | 10 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0245 others(7): Show |
10 | HG02004.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.239+31690C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505578 | |||||||
chr4:153505784 | T | C | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+31896T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505784 | |||||||
chr4:153505868 | A | G | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+31980A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505868 | |||||||
chr4:153505954 | C | T | 1 | a0001c0012t0001g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.239+32066C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153505954 | |||||||
chr4:153506092 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
75 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.239+32204G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506092 | |||||||
chr4:153506167 | A | G | 90 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
90 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.239+32279A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506167 | |||||||
chr4:153506285 | G | T | 1 | a0001c0001t0001g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.239+32397G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506285 | |||||||
chr4:153506296 | C | T | 4 | a0001c0005t0001g0022 a0002c0010t0001g0021 a0002c0057t0001g0032 others(1): Show |
4 | HG02922.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+32408C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506296 | |||||||
chr4:153506418 | C | T | 1 | a0001c0020t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.239+32530C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506418 | |||||||
chr4:153506500 | A | G | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+32612A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506500 | |||||||
chr4:153506595 | C | A | 2 | a0001c0003t0001g0181 a0001c0003t0001g0201 |
2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.239+32707C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506595 | |||||||
chr4:153506612 | G | A | 3 | a0001c0001t0001g0086 a0001c0005t0003g0034 a0011c0035t0001g0035 |
3 | HG02615.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+32724G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506612 | |||||||
chr4:153506757 | C | T | 7 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0245 others(4): Show |
7 | HG02896.hp2 HG02897.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+32869C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506757 | |||||||
chr4:153506791 | C | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(77): Show |
80 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.239+32903C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506791 | |||||||
chr4:153506815 | C | T | 10 | a0001c0002t0001g0113 a0001c0003t0001g0181 a0001c0003t0001g0201 others(7): Show |
10 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.239+32927C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506815 | |||||||
chr4:153506843 | CA | C | 9 | a0001c0001t0001g0039 a0001c0002t0001g0100 a0001c0005t0001g0038 others(6): Show |
9 | HG01243.hp2 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+32973delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153506843 | ||||||
chr4:153506843 | CAA | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(75): Show |
78 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.239+32972_239+3297 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153506843 | ||||||
chr4:153506843 | CAAA | C | 8 | a0001c0001t0001g0227 a0001c0005t0001g0022 a0001c0014t0001g0155 others(5): Show |
8 | HG02273.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+32971_239+3297 others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153506843 | ||||||
chr4:153506852 | A | G | 3 | a0001c0005t0001g0106 a0001c0028t0001g0108 a0003c0023t0001g0107 |
3 | HG01884.hp2 HG02148.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.239+32964A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506852 | |||||||
chr4:153506960 | A | G | 13 | a0001c0002t0001g0060 a0001c0003t0001g0178 a0001c0003t0001g0206 others(10): Show |
13 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.239+33072A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153506960 | |||||||
chr4:153507516 | C | T | 2 | a0001c0001t0001g0039 a0005c0017t0001g0040 |
2 | HG01243.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.239+33628C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153507516 | |||||||
chr4:153507517 | G | A | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+33629G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153507517 | |||||||
chr4:153507591 | G | A | 3 | a0001c0001t0001g0086 a0001c0005t0003g0034 a0001c0013t0001g0088 |
3 | HG04199.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+33703G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153507591 | |||||||
chr4:153507720 | AAAAC | A | 4 | a0001c0004t0001g0146 a0001c0004t0001g0147 a0001c0004t0001g0148 others(1): Show |
4 | NA18955.hp2 NA18960.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+33844_239+3384 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153507720 | ||||||
chr4:153507868 | C | G | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+33980C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153507868 | |||||||
chr4:153507970 | G | A | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+34082G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153507970 | |||||||
chr4:153508360 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.239+34472T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508360 | |||||||
chr4:153508403 | C | T | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
75 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.239+34515C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508403 | |||||||
chr4:153508561 | C | A | 4 | a0001c0005t0001g0022 a0002c0010t0001g0021 a0002c0057t0001g0032 others(1): Show |
4 | HG02922.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+34673C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508561 | |||||||
chr4:153508579 | A | T | 5 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+34691A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508579 | |||||||
chr4:153508636 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
75 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.239+34748G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508636 | |||||||
chr4:153508668 | T | G | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+34780T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508668 | |||||||
chr4:153508678 | A | AT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0227 a0001c0001t0002g0061 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.239+34807dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153508678 | ||||||
chr4:153508785 | C | T | 3 | a0001c0003t0001g0122 a0001c0004t0001g0125 a0001c0012t0001g0126 |
3 | HG00140.hp1 HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.239+34897C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508785 | |||||||
chr4:153508801 | C | T | 1 | a0001c0005t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.239+34913C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508801 | |||||||
chr4:153508802 | G | A | 10 | a0001c0003t0001g0157 a0001c0003t0001g0163 a0001c0003t0001g0239 others(7): Show |
10 | HG00544.hp2 HG00597.hp2 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.239+34914G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508802 | |||||||
chr4:153508844 | A | G | 4 | a0001c0001t0001g0025 a0001c0005t0001g0247 a0004c0027t0001g0248 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+34956A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508844 | |||||||
chr4:153508890 | C | T | 56 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(53): Show |
56 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.239+35002C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153508890 | |||||||
chr4:153509197 | C | A | 2 | a0001c0003t0001g0157 a0001c0009t0001g0158 |
2 | HG00597.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.239+35309C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153509197 | |||||||
chr4:153509197 | CA | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(96): Show |
99 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.239+35317delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153509197 | ||||||
chr4:153509224 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
75 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.239+35336G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153509224 | |||||||
chr4:153509365 | CA | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(90): Show |
93 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.239+35489delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153509365 | ||||||
chr4:153509696 | G | A | 2 | a0001c0009t0001g0145 a0001c0034t0001g0020 |
2 | NA18906.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.239+35808G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153509696 | |||||||
chr4:153509726 | C | T | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+35838C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153509726 | |||||||
chr4:153509913 | A | G | 2 | a0005c0017t0001g0026 a0005c0017t0001g0027 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.239+36025A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153509913 | |||||||
chr4:153510165 | T | G | 9 | a0001c0001t0001g0227 a0001c0002t0001g0245 a0001c0002t0001g0246 others(6): Show |
9 | HG02559.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+36277T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153510165 | |||||||
chr4:153510253 | A | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0005t0001g0038 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+36365A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153510253 | |||||||
chr4:153510494 | G | A | 2 | a0001c0003t0001g0196 a0002c0016t0001g0215 |
2 | HG00735.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.239+36606G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153510494 | |||||||
chr4:153510529 | A | G | 1 | a0001c0001t0001g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.239+36641A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153510529 | |||||||
chr4:153510637 | G | C | 1 | a0001c0013t0001g0090 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.239+36749G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153510637 | |||||||
chr4:153510668 | A | G | 3 | a0001c0001t0001g0086 a0001c0005t0003g0034 a0011c0035t0001g0035 |
3 | HG02615.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239+36780A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153510668 | |||||||
chr4:153510745 | G | C | 13 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0002t0001g0017 others(10): Show |
13 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.239+36857G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153510745 | |||||||
chr4:153510873 | T | A | 1 | a0001c0008t0001g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.239+36985T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153510873 | |||||||
chr4:153510886 | C | CA | 8 | a0001c0002t0001g0100 a0001c0002t0001g0213 a0001c0003t0001g0161 others(5): Show |
8 | HG00408.hp2 HG00544.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+37009dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153510886 | ||||||
chr4:153511053 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.239+37165C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511053 | |||||||
chr4:153511118 | A | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
75 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.239+37230A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511118 | |||||||
chr4:153511149 | A | G | 13 | a0001c0001t0001g0008 a0001c0002t0001g0002 a0001c0002t0001g0005 others(10): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.239+37261A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511149 | |||||||
chr4:153511276 | A | C | 10 | a0001c0001t0001g0039 a0001c0002t0001g0017 a0001c0002t0001g0019 others(7): Show |
10 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.239+37388A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511276 | |||||||
chr4:153511282 | C | T | 1 | a0001c0037t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.239+37394C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511282 | |||||||
chr4:153511283 | G | A | 2 | a0001c0021t0001g0037 a0008c0052t0001g0120 |
2 | HG02572.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.239+37395G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511283 | |||||||
chr4:153511330 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
75 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.239+37442G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511330 | |||||||
chr4:153511460 | A | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(84): Show |
87 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.239+37572A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511460 | |||||||
chr4:153511576 | C | T | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.239+37688C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511576 | |||||||
chr4:153511597 | C | T | 1 | a0001c0014t0001g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.239+37709C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511597 | |||||||
chr4:153511663 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.239+37775C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511663 | |||||||
chr4:153511826 | A | G | 1 | a0001c0003t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.239+37938A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153511826 | |||||||
chr4:153512072 | G | A | 5 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-38001G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153512072 | |||||||
chr4:153512090 | CTTT | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(99): Show |
102 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.240-37981_240-3797 others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153512090 | ||||||
chr4:153512205 | T | G | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-37868T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153512205 | |||||||
chr4:153512713 | A | C | 58 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(55): Show |
58 | HG00597.hp1 HG01070.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.240-37360A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153512713 | |||||||
chr4:153512787 | G | A | 2 | a0001c0005t0001g0106 a0001c0028t0001g0108 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.240-37286G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153512787 | |||||||
chr4:153512811 | A | G | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-37262A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153512811 | |||||||
chr4:153512833 | C | T | 57 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0042 others(54): Show |
57 | HG00597.hp1 HG01070.hp2 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.240-37240C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153512833 | |||||||
chr4:153512869 | C | T | 4 | a0001c0001t0001g0025 a0001c0005t0001g0247 a0004c0027t0001g0248 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-37204C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153512869 | |||||||
chr4:153513213 | C | T | 2 | a0001c0003t0001g0157 a0001c0009t0001g0158 |
2 | HG00597.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.240-36860C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513213 | |||||||
chr4:153513355 | T | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.240-36718T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513355 | |||||||
chr4:153513501 | C | T | 1 | a0001c0008t0001g0184 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.240-36572C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513501 | |||||||
chr4:153513611 | G | A | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.240-36462G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513611 | |||||||
chr4:153513692 | T | C | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.240-36381T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513692 | |||||||
chr4:153513735 | A | G | 1 | a0003c0019t0001g0154 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.240-36338A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513735 | |||||||
chr4:153513830 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.240-36243T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513830 | |||||||
chr4:153513913 | G | A | 2 | a0001c0003t0001g0181 a0001c0003t0001g0201 |
2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.240-36160G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513913 | |||||||
chr4:153513940 | A | C | 3 | a0001c0012t0001g0205 a0002c0006t0001g0202 a0002c0006t0001g0203 |
3 | HG01496.hp2 HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.240-36133A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513940 | |||||||
chr4:153513965 | T | G | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.240-36108T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153513965 | |||||||
chr4:153514219 | A | T | 5 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0005t0001g0106 others(2): Show |
5 | HG01884.hp2 HG02148.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-35854A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153514219 | |||||||
chr4:153514389 | T | C | 1 | a0001c0005t0003g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.240-35684T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153514389 | |||||||
chr4:153514602 | T | C | 5 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-35471T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153514602 | |||||||
chr4:153514696 | T | G | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-35377T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153514696 | |||||||
chr4:153514820 | C | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(47): Show |
50 | HG01243.hp2 HG01255.hp1 HG01891.hp2 others(47): Show |
intron_variant | MODIFIER | c.240-35253C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153514820 | |||||||
chr4:153514820 | C | T | 2 | a0001c0056t0001g0160 a0011c0035t0001g0035 |
2 | HG02615.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.240-35253C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153514820 | |||||||
chr4:153514873 | C | T | 2 | a0001c0009t0001g0175 a0002c0007t0001g0084 |
2 | NA18940.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.240-35200C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153514873 | |||||||
chr4:153514924 | G | A | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-35149G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153514924 | |||||||
chr4:153515299 | C | T | 5 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0005t0001g0106 others(2): Show |
5 | HG01884.hp2 HG02148.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-34774C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153515299 | |||||||
chr4:153515573 | A | G | 3 | a0001c0003t0001g0117 a0001c0003t0001g0172 a0001c0003t0001g0173 |
3 | NA18981.hp2 NA18983.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.240-34500A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153515573 | |||||||
chr4:153515756 | G | A | 6 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-34317G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153515756 | |||||||
chr4:153515912 | A | AT | 44 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0003t0001g0122 others(41): Show |
44 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.240-34146dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153515912 | ||||||
chr4:153515912 | AT | A | 15 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0086 others(12): Show |
15 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.240-34146delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153515912 | ||||||
chr4:153516274 | G | C | 1 | a0001c0037t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.240-33799G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516274 | |||||||
chr4:153516444 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.240-33629C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516444 | |||||||
chr4:153516460 | G | A | 8 | a0001c0001t0001g0227 a0001c0002t0001g0245 a0001c0002t0001g0246 others(5): Show |
8 | HG01884.hp2 HG02148.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-33613G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516460 | |||||||
chr4:153516537 | C | T | 8 | a0001c0001t0001g0227 a0001c0002t0001g0245 a0001c0002t0001g0246 others(5): Show |
8 | HG01884.hp2 HG02148.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-33536C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516537 | |||||||
chr4:153516565 | A | G | 1 | a0001c0008t0001g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.240-33508A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516565 | |||||||
chr4:153516711 | A | G | 56 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(53): Show |
56 | HG00597.hp1 HG01070.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.240-33362A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516711 | |||||||
chr4:153516792 | G | C | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-33281G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516792 | |||||||
chr4:153516866 | C | T | 4 | a0001c0001t0001g0025 a0001c0005t0001g0247 a0004c0027t0001g0248 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-33207C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516866 | |||||||
chr4:153516919 | C | T | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.240-33154C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516919 | |||||||
chr4:153516981 | C | T | 17 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0086 others(14): Show |
17 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.240-33092C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153516981 | |||||||
chr4:153517076 | C | T | 5 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0005t0001g0106 others(2): Show |
5 | HG01884.hp2 HG02148.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-32997C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153517076 | |||||||
chr4:153517330 | T | C | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-32743T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153517330 | |||||||
chr4:153517404 | G | A | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.240-32669G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153517404 | |||||||
chr4:153517470 | A | AT | 5 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-32594dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153517470 | ||||||
chr4:153517470 | AT | A | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.240-32594delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153517470 | ||||||
chr4:153517575 | G | A | 1 | a0001c0003t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.240-32498G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153517575 | |||||||
chr4:153517700 | A | G | 3 | a0001c0012t0001g0205 a0002c0006t0001g0202 a0002c0006t0001g0203 |
3 | HG01496.hp2 HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.240-32373A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153517700 | |||||||
chr4:153517722 | G | A | 2 | a0001c0002t0001g0045 a0002c0015t0001g0046 |
2 | NA18953.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.240-32351G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153517722 | |||||||
chr4:153517851 | C | T | 6 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-32222C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153517851 | |||||||
chr4:153518032 | GA | G | 12 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0086 others(9): Show |
12 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.240-32031delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153518032 | ||||||
chr4:153518311 | C | T | 5 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-31762C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153518311 | |||||||
chr4:153518400 | T | C | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.240-31673T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153518400 | |||||||
chr4:153518534 | A | ACC | 38 | a0001c0003t0001g0122 a0001c0003t0001g0133 a0001c0003t0001g0141 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.240-31538_240-3153 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153518534 | ||||||
chr4:153518662 | A | G | 1 | a0001c0005t0002g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.240-31411A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153518662 | |||||||
chr4:153518724 | G | A | 2 | a0001c0056t0001g0160 a0002c0015t0001g0018 |
2 | NA18978.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.240-31349G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153518724 | |||||||
chr4:153518753 | T | TTGGTGCT others(7): Show |
1 | a0002c0055t0001g0207 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.240-31317_240-3130 others(18): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153518753 | ||||||
chr4:153518864 | C | G | 1 | a0001c0011t0001g0243 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.240-31209C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153518864 | |||||||
chr4:153518965 | T | C | 1 | a0001c0059t0001g0033 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.240-31108T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153518965 | |||||||
chr4:153518967 | C | T | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-31106C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153518967 | |||||||
chr4:153518983 | C | A | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.240-31090C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153518983 | |||||||
chr4:153519036 | A | G | 7 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(4): Show |
7 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.240-31037A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519036 | |||||||
chr4:153519193 | T | G | 1 | a0001c0004t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.240-30880T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519193 | |||||||
chr4:153519300 | C | G | 3 | a0001c0005t0001g0106 a0001c0028t0001g0108 a0003c0023t0001g0107 |
3 | HG01884.hp2 HG02148.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.240-30773C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519300 | |||||||
chr4:153519563 | T | C | 5 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-30510T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519563 | |||||||
chr4:153519621 | C | A | 3 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0002c0006t0001g0242 |
3 | HG03017.hp1 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.240-30452C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519621 | |||||||
chr4:153519701 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(40): Show |
43 | HG01243.hp2 HG01255.hp1 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.240-30372G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519701 | |||||||
chr4:153519864 | A | T | 2 | a0002c0007t0001g0071 a0002c0007t0001g0072 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.240-30209A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519864 | |||||||
chr4:153519999 | T | C | 63 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0058 others(60): Show |
63 | HG00597.hp1 HG01070.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.240-30074T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519999 | |||||||
chr4:153519999 | T | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(95): Show |
98 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.240-30074T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153519999 | |||||||
chr4:153520007 | CCA | C | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.240-30065_240-3006 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520007 | |||||||
chr4:153520055 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.240-30018C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520055 | |||||||
chr4:153520056 | A | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(152): Show |
155 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.240-30017A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520056 | |||||||
chr4:153520101 | C | T | 1 | a0002c0025t0001g0166 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.240-29972C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520101 | |||||||
chr4:153520179 | C | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0217 |
3 | HG02486.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.240-29894C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520179 | |||||||
chr4:153520192 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.240-29881C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520192 | |||||||
chr4:153520390 | T | G | 93 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(90): Show |
93 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.240-29683T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520390 | |||||||
chr4:153520394 | T | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(90): Show |
93 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.240-29679T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520394 | |||||||
chr4:153520476 | T | G | 1 | a0001c0002t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.240-29597T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520476 | |||||||
chr4:153520654 | G | A | 1 | a0001c0009t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.240-29419G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520654 | |||||||
chr4:153520696 | T | C | 4 | a0001c0004t0001g0146 a0001c0004t0001g0147 a0001c0004t0001g0148 others(1): Show |
4 | NA18955.hp2 NA18960.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-29377T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520696 | |||||||
chr4:153520817 | C | T | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0056t0001g0160 others(2): Show |
5 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-29256C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520817 | |||||||
chr4:153520842 | A | G | 4 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-29231A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520842 | |||||||
chr4:153520884 | T | C | 5 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0005t0001g0106 others(2): Show |
5 | HG01884.hp2 HG02148.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-29189T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153520884 | |||||||
chr4:153521173 | G | T | 1 | a0001c0002t0001g0057 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.240-28900G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521173 | |||||||
chr4:153521335 | C | T | 1 | a0002c0016t0001g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.240-28738C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521335 | |||||||
chr4:153521353 | C | A | 59 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0089 others(56): Show |
59 | HG00597.hp1 HG01070.hp2 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.240-28720C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521353 | |||||||
chr4:153521430 | C | T | 4 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-28643C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521430 | |||||||
chr4:153521448 | T | C | 6 | a0001c0001t0001g0025 a0001c0002t0001g0007 a0001c0002t0002g0080 others(3): Show |
6 | HG02258.hp1 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.240-28625T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521448 | |||||||
chr4:153521611 | G | A | 1 | a0001c0008t0001g0199 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.240-28462G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521611 | |||||||
chr4:153521627 | A | G | 1 | a0001c0009t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.240-28446A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521627 | |||||||
chr4:153521844 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-28229G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521844 | |||||||
chr4:153521862 | G | GT | 6 | a0001c0004t0001g0193 a0001c0004t0001g0197 a0001c0004t0001g0240 others(3): Show |
6 | HG03098.hp2 NA18952.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.240-28195dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153521862 | ||||||
chr4:153521862 | GTT | G | 143 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(140): Show |
143 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.240-28196_240-2819 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153521862 | ||||||
chr4:153521862 | GTTT | G | 8 | a0001c0002t0001g0005 a0001c0011t0001g0243 a0002c0010t0001g0073 others(5): Show |
8 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.240-28197_240-2819 others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153521862 | ||||||
chr4:153521865 | T | G | 1 | a0001c0001t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.240-28208T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521865 | |||||||
chr4:153521866 | T | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(18): Show |
21 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-28207T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521866 | |||||||
chr4:153521969 | C | T | 55 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0089 others(52): Show |
55 | HG00597.hp1 HG01070.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.240-28104C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153521969 | |||||||
chr4:153522494 | G | A | 83 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0001t0001g0223 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.240-27579G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153522494 | |||||||
chr4:153522633 | C | G | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-27440C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153522633 | |||||||
chr4:153522823 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.240-27250C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153522823 | |||||||
chr4:153522881 | C | T | 1 | a0002c0025t0001g0166 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.240-27192C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153522881 | |||||||
chr4:153522923 | T | C | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-27150T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153522923 | |||||||
chr4:153522966 | A | G | 1 | a0002c0045t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.240-27107A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153522966 | |||||||
chr4:153523023 | A | G | 1 | a0003c0023t0001g0107 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.240-27050A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523023 | |||||||
chr4:153523052 | G | A | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-27021G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523052 | |||||||
chr4:153523324 | G | C | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-26749G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523324 | |||||||
chr4:153523420 | CCAGAGAG others(3): Show |
C | 1 | a0002c0006t0001g0130 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.240-26650_240-2664 others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153523420 | ||||||
chr4:153523566 | C | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-26507C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523566 | |||||||
chr4:153523625 | G | A | 4 | a0001c0001t0001g0244 a0001c0008t0001g0128 a0001c0008t0001g0129 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-26448G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523625 | |||||||
chr4:153523632 | TG | T | 4 | a0001c0013t0001g0088 a0001c0056t0001g0160 a0002c0006t0001g0242 others(1): Show |
4 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-26438delG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153523632 | ||||||
chr4:153523665 | T | C | 13 | a0001c0003t0001g0157 a0001c0003t0001g0178 a0001c0003t0001g0206 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.240-26408T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523665 | |||||||
chr4:153523725 | T | G | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-26348T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523725 | |||||||
chr4:153523786 | C | T | 1 | a0001c0009t0001g0192 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.240-26287C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523786 | |||||||
chr4:153523839 | G | A | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-26234G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523839 | |||||||
chr4:153523913 | C | T | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-26160C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523913 | |||||||
chr4:153523934 | T | C | 1 | a0001c0014t0001g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.240-26139T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153523934 | |||||||
chr4:153524028 | G | T | 1 | a0001c0005t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.240-26045G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524028 | |||||||
chr4:153524059 | A | G | 14 | a0001c0003t0001g0157 a0001c0003t0001g0178 a0001c0003t0001g0206 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.240-26014A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524059 | |||||||
chr4:153524131 | GT | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
48 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.240-25922delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153524131 | ||||||
chr4:153524131 | GTT | G | 53 | a0001c0001t0001g0086 a0001c0002t0001g0002 a0001c0002t0001g0005 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.240-25923_240-2592 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153524131 | ||||||
chr4:153524152 | C | T | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.240-25921C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524152 | |||||||
chr4:153524154 | T | C | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.240-25919T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524154 | |||||||
chr4:153524209 | A | G | 1 | a0001c0008t0001g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.240-25864A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524209 | |||||||
chr4:153524243 | C | T | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-25830C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524243 | |||||||
chr4:153524292 | G | A | 4 | a0001c0013t0001g0088 a0001c0056t0001g0160 a0002c0006t0001g0242 others(1): Show |
4 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-25781G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524292 | |||||||
chr4:153524375 | C | A | 52 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0002t0001g0002 others(49): Show |
52 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.240-25698C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524375 | |||||||
chr4:153524446 | T | C | 39 | a0001c0001t0001g0086 a0001c0003t0001g0133 a0001c0003t0001g0141 others(36): Show |
39 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.240-25627T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524446 | |||||||
chr4:153524455 | A | G | 4 | a0001c0003t0001g0124 a0002c0007t0001g0070 a0002c0045t0001g0121 others(1): Show |
4 | HG01099.hp1 HG01109.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-25618A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524455 | |||||||
chr4:153524581 | G | A | 1 | a0001c0009t0001g0177 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.240-25492G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153524581 | |||||||
chr4:153525187 | C | G | 88 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0001t0001g0223 others(85): Show |
88 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.240-24886C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525187 | |||||||
chr4:153525340 | T | C | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-24733T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525340 | |||||||
chr4:153525467 | G | A | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-24606G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525467 | |||||||
chr4:153525530 | G | T | 4 | a0001c0013t0001g0088 a0001c0056t0001g0160 a0002c0006t0001g0242 others(1): Show |
4 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-24543G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525530 | |||||||
chr4:153525572 | T | G | 2 | a0001c0005t0001g0106 a0001c0028t0001g0108 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.240-24501T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525572 | |||||||
chr4:153525582 | A | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-24491A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525582 | |||||||
chr4:153525685 | T | C | 92 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0001t0001g0223 others(89): Show |
92 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.240-24388T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525685 | |||||||
chr4:153525713 | A | G | 12 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(9): Show |
12 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.240-24360A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525713 | |||||||
chr4:153525835 | C | T | 1 | a0001c0002t0001g0057 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.240-24238C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525835 | |||||||
chr4:153525865 | A | AT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(12): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.240-24198dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153525865 | ||||||
chr4:153525926 | G | A | 4 | a0001c0013t0001g0088 a0001c0056t0001g0160 a0002c0006t0001g0242 others(1): Show |
4 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-24147G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153525926 | |||||||
chr4:153526046 | A | G | 1 | a0001c0002t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.240-24027A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526046 | |||||||
chr4:153526104 | A | G | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240-23969A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526104 | |||||||
chr4:153526271 | C | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-23802C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526271 | |||||||
chr4:153526423 | A | G | 1 | a0001c0047t0001g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.240-23650A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526423 | |||||||
chr4:153526503 | G | A | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-23570G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526503 | |||||||
chr4:153526541 | C | T | 4 | a0001c0013t0001g0088 a0001c0056t0001g0160 a0002c0006t0001g0242 others(1): Show |
4 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-23532C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526541 | |||||||
chr4:153526655 | G | A | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-23418G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526655 | |||||||
chr4:153526663 | G | A | 3 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 |
3 | HG01243.hp2 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.240-23410G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526663 | |||||||
chr4:153526693 | C | T | 52 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0002t0001g0002 others(49): Show |
52 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.240-23380C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526693 | |||||||
chr4:153526736 | C | CA | 5 | a0001c0009t0001g0170 a0002c0006t0001g0130 a0002c0010t0001g0069 others(2): Show |
5 | HG00558.hp2 NA18972.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-23324dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153526736 | ||||||
chr4:153526758 | G | A | 36 | a0001c0003t0001g0133 a0001c0003t0001g0141 a0001c0004t0001g0115 others(33): Show |
36 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.240-23315G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153526758 | |||||||
chr4:153527008 | G | A | 1 | a0001c0002t0001g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.240-23065G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527008 | |||||||
chr4:153527065 | C | CTT | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-23004_240-2300 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153527065 | ||||||
chr4:153527201 | T | C | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-22872T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527201 | |||||||
chr4:153527267 | GT | G | 71 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0002t0001g0002 others(68): Show |
71 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.240-22798delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153527267 | ||||||
chr4:153527281 | T | TG | 14 | a0001c0003t0001g0157 a0001c0003t0001g0161 a0001c0003t0001g0178 others(11): Show |
14 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.240-22785dupG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153527281 | ||||||
chr4:153527282 | G | T | 53 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0002t0001g0002 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.240-22791G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527282 | |||||||
chr4:153527328 | AGT | A | 19 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
19 | HG01884.hp2 HG02148.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.240-22743_240-2274 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153527328 | ||||||
chr4:153527335 | C | T | 2 | a0001c0001t0001g0086 a0001c0005t0003g0034 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.240-22738C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527335 | |||||||
chr4:153527358 | C | T | 1 | a0003c0019t0001g0154 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.240-22715C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527358 | |||||||
chr4:153527393 | C | T | 2 | a0001c0001t0001g0089 a0001c0002t0001g0092 |
2 | NA18944.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.240-22680C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527393 | |||||||
chr4:153527451 | C | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-22622C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527451 | |||||||
chr4:153527461 | G | A | 4 | a0001c0013t0001g0088 a0001c0056t0001g0160 a0002c0006t0001g0242 others(1): Show |
4 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-22612G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527461 | |||||||
chr4:153527636 | C | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-22437C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527636 | |||||||
chr4:153527720 | G | T | 86 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0001t0001g0223 others(83): Show |
86 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.240-22353G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527720 | |||||||
chr4:153527741 | C | T | 1 | a0001c0004t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.240-22332C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527741 | |||||||
chr4:153527789 | T | G | 1 | a0001c0037t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.240-22284T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527789 | |||||||
chr4:153527876 | A | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-22197A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527876 | |||||||
chr4:153527935 | A | G | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-22138A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153527935 | |||||||
chr4:153528008 | C | A | 1 | a0002c0010t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.240-22065C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153528008 | |||||||
chr4:153528087 | C | G | 3 | a0001c0001t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | HG02559.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.240-21986C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153528087 | |||||||
chr4:153528160 | T | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(18): Show |
21 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-21913T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153528160 | |||||||
chr4:153528166 | A | G | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-21907A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153528166 | |||||||
chr4:153528361 | T | A | 6 | a0001c0002t0001g0024 a0001c0005t0001g0232 a0001c0013t0001g0088 others(3): Show |
6 | HG01891.hp1 HG03209.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.240-21712T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153528361 | |||||||
chr4:153528367 | A | C | 4 | a0001c0005t0001g0022 a0002c0010t0001g0021 a0002c0057t0001g0032 others(1): Show |
4 | HG02922.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-21706A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153528367 | |||||||
chr4:153528479 | T | C | 4 | a0001c0013t0001g0088 a0001c0056t0001g0160 a0002c0006t0001g0242 others(1): Show |
4 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-21594T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153528479 | |||||||
chr4:153528600 | GT | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0219 a0001c0001t0001g0222 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-21468delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153528600 | ||||||
chr4:153528944 | T | C | 152 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(149): Show |
152 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.240-21129T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153528944 | |||||||
chr4:153529081 | G | A | 1 | a0002c0048t0001g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.240-20992G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153529081 | |||||||
chr4:153529260 | T | G | 4 | a0001c0005t0001g0022 a0002c0010t0001g0021 a0002c0057t0001g0032 others(1): Show |
4 | HG02922.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-20813T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153529260 | |||||||
chr4:153529472 | T | C | 10 | a0001c0001t0001g0008 a0001c0005t0001g0022 a0001c0008t0001g0204 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.240-20601T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153529472 | |||||||
chr4:153529665 | G | T | 39 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0002t0001g0245 others(36): Show |
39 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.240-20408G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153529665 | |||||||
chr4:153529688 | G | T | 5 | a0001c0013t0001g0049 a0001c0013t0001g0088 a0001c0056t0001g0160 others(2): Show |
5 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-20385G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153529688 | |||||||
chr4:153529748 | A | G | 13 | a0001c0002t0001g0024 a0001c0002t0001g0100 a0001c0002t0001g0245 others(10): Show |
13 | HG01891.hp1 HG02145.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.240-20325A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153529748 | |||||||
chr4:153529808 | T | A | 46 | a0001c0001t0001g0086 a0001c0002t0001g0024 a0001c0002t0001g0100 others(43): Show |
46 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.240-20265T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153529808 | |||||||
chr4:153529921 | C | T | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-20152C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153529921 | |||||||
chr4:153530033 | C | CT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0008t0001g0204 others(6): Show |
9 | HG01255.hp1 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.240-20025dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153530033 | ||||||
chr4:153530033 | CT | C | 10 | a0001c0002t0001g0024 a0001c0002t0001g0100 a0001c0002t0001g0245 others(7): Show |
10 | HG01891.hp1 HG02145.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.240-20025delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153530033 | ||||||
chr4:153530228 | G | C | 1 | a0001c0037t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.240-19845G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153530228 | |||||||
chr4:153530246 | T | C | 7 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(4): Show |
7 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.240-19827T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153530246 | |||||||
chr4:153530361 | A | G | 9 | a0001c0002t0001g0024 a0001c0002t0001g0100 a0001c0005t0001g0232 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.240-19712A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153530361 | |||||||
chr4:153530526 | A | C | 36 | a0001c0001t0001g0086 a0001c0003t0001g0133 a0001c0003t0001g0141 others(33): Show |
36 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.240-19547A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153530526 | |||||||
chr4:153530571 | G | C | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-19502G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153530571 | |||||||
chr4:153530683 | AT | A | 9 | a0001c0002t0001g0024 a0001c0002t0001g0100 a0001c0005t0001g0232 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.240-19387delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153530683 | ||||||
chr4:153530730 | A | G | 9 | a0001c0002t0001g0024 a0001c0002t0001g0100 a0001c0005t0001g0232 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.240-19343A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153530730 | |||||||
chr4:153530816 | C | T | 1 | a0001c0013t0001g0087 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.240-19257C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153530816 | |||||||
chr4:153530946 | A | G | 1 | a0001c0004t0001g0143 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.240-19127A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153530946 | |||||||
chr4:153531096 | G | T | 36 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(33): Show |
36 | HG01081.hp1 HG01123.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.240-18977G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153531096 | |||||||
chr4:153531192 | A | C | 1 | a0001c0008t0001g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.240-18881A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153531192 | |||||||
chr4:153531195 | TATTCCTC others(8): Show |
T | 2 | a0001c0004t0001g0135 a0001c0004t0001g0137 |
2 | NA18953.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.240-18871_240-1885 others(19): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153531195 | ||||||
chr4:153531382 | G | C | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-18691G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153531382 | |||||||
chr4:153531587 | C | G | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-18486C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153531587 | |||||||
chr4:153531619 | C | T | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-18454C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153531619 | |||||||
chr4:153531800 | C | G | 81 | a0001c0001t0001g0086 a0001c0001t0001g0223 a0001c0001t0001g0224 others(78): Show |
81 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.240-18273C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153531800 | |||||||
chr4:153532080 | G | T | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240-17993G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532080 | |||||||
chr4:153532329 | C | T | 7 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(4): Show |
7 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.240-17744C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532329 | |||||||
chr4:153532437 | CT | C | 6 | a0001c0002t0001g0024 a0001c0004t0001g0146 a0001c0005t0001g0232 others(3): Show |
6 | HG01891.hp1 HG01993.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-17627delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153532437 | ||||||
chr4:153532445 | T | A | 5 | a0001c0013t0001g0049 a0001c0013t0001g0088 a0001c0056t0001g0160 others(2): Show |
5 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-17628T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532445 | |||||||
chr4:153532445 | T | TA | 14 | a0001c0002t0001g0076 a0001c0003t0001g0157 a0001c0003t0001g0178 others(11): Show |
14 | HG01123.hp2 HG01192.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.240-17628_240-1762 others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532445 | |||||||
chr4:153532446 | T | A | 63 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0001t0001g0223 others(60): Show |
63 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.240-17627T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532446 | |||||||
chr4:153532446 | T | TA | 17 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(14): Show |
17 | HG01884.hp2 HG02109.hp2 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.240-17614dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153532446 | ||||||
chr4:153532446 | TA | T | 8 | a0001c0002t0001g0045 a0001c0002t0001g0245 a0001c0002t0001g0246 others(5): Show |
8 | HG01070.hp1 HG01070.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-17614delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153532446 | ||||||
chr4:153532447 | A | T | 3 | a0001c0001t0001g0039 a0001c0005t0001g0038 a0001c0021t0001g0037 |
3 | HG01243.hp2 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.240-17626A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532447 | |||||||
chr4:153532485 | G | A | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-17588G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532485 | |||||||
chr4:153532489 | A | G | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-17584A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532489 | |||||||
chr4:153532640 | C | T | 1 | a0002c0016t0001g0191 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.240-17433C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532640 | |||||||
chr4:153532684 | A | T | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-17389A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532684 | |||||||
chr4:153532771 | G | A | 3 | a0001c0024t0001g0010 a0001c0034t0001g0020 a0004c0027t0001g0248 |
3 | HG02280.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.240-17302G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532771 | |||||||
chr4:153532974 | T | A | 1 | a0001c0002t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.240-17099T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153532974 | |||||||
chr4:153532984 | C | CT | 31 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(28): Show |
31 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.240-17071dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153532984 | ||||||
chr4:153532984 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0001g0100 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.240-17085_240-1707 others(19): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153532984 | ||||||
chr4:153532984 | C | CTTTTTTT others(9): Show |
1 | a0001c0033t0001g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.240-17086_240-1707 others(20): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153532984 | ||||||
chr4:153533015 | C | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-17058C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533015 | |||||||
chr4:153533183 | C | G | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240-16890C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533183 | |||||||
chr4:153533232 | G | T | 2 | a0001c0001t0001g0008 a0001c0021t0001g0014 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.240-16841G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533232 | |||||||
chr4:153533264 | C | T | 1 | a0002c0006t0001g0186 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.240-16809C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533264 | |||||||
chr4:153533385 | G | A | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-16688G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533385 | |||||||
chr4:153533552 | A | G | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-16521A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533552 | |||||||
chr4:153533553 | A | T | 5 | a0001c0013t0001g0049 a0001c0013t0001g0088 a0001c0056t0001g0160 others(2): Show |
5 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-16520A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533553 | |||||||
chr4:153533631 | C | A | 5 | a0001c0013t0001g0049 a0001c0013t0001g0088 a0001c0056t0001g0160 others(2): Show |
5 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-16442C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533631 | |||||||
chr4:153533646 | G | C | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-16427G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533646 | |||||||
chr4:153533676 | T | A | 1 | a0002c0039t0001g0053 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.240-16397T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533676 | |||||||
chr4:153533742 | T | C | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-16331T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153533742 | |||||||
chr4:153534088 | A | C | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-15985A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534088 | |||||||
chr4:153534136 | G | A | 5 | a0001c0013t0001g0049 a0001c0013t0001g0088 a0001c0056t0001g0160 others(2): Show |
5 | HG03654.hp1 HG04199.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-15937G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534136 | |||||||
chr4:153534163 | C | T | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-15910C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534163 | |||||||
chr4:153534580 | T | C | 3 | a0001c0002t0001g0009 a0001c0002t0001g0100 a0001c0033t0001g0099 |
3 | HG02145.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.240-15493T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534580 | |||||||
chr4:153534594 | C | T | 2 | a0001c0002t0001g0054 a0014c0042t0001g0001 |
2 | HG02071.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.240-15479C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534594 | |||||||
chr4:153534651 | T | A | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.240-15422T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534651 | |||||||
chr4:153534675 | C | G | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-15398C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534675 | |||||||
chr4:153534695 | T | A | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-15378T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534695 | |||||||
chr4:153534724 | C | T | 5 | a0001c0001t0001g0025 a0001c0024t0001g0010 a0001c0034t0001g0020 others(2): Show |
5 | HG01255.hp1 HG02280.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-15349C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534724 | |||||||
chr4:153534893 | G | A | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.240-15180G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534893 | |||||||
chr4:153534897 | C | T | 2 | a0001c0002t0001g0024 a0001c0005t0001g0232 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240-15176C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534897 | |||||||
chr4:153534898 | G | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(115): Show |
118 | HG00140.hp1 HG00609.hp1 HG01123.hp2 others(115): Show |
intron_variant | MODIFIER | c.240-15175G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534898 | |||||||
chr4:153534900 | G | A | 3 | a0001c0002t0001g0009 a0001c0002t0001g0100 a0001c0033t0001g0099 |
3 | HG02145.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.240-15173G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153534900 | |||||||
chr4:153535003 | G | A | 14 | a0001c0002t0001g0076 a0001c0003t0001g0157 a0001c0003t0001g0178 others(11): Show |
14 | HG01081.hp1 HG01123.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.240-15070G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535003 | |||||||
chr4:153535176 | T | C | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-14897T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535176 | |||||||
chr4:153535302 | C | T | 1 | a0001c0012t0001g0126 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.240-14771C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535302 | |||||||
chr4:153535421 | T | C | 1 | a0002c0010t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.240-14652T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535421 | |||||||
chr4:153535700 | A | G | 21 | a0001c0003t0001g0141 a0001c0003t0001g0239 a0001c0004t0001g0125 others(18): Show |
21 | HG00140.hp1 HG00609.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-14373A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535700 | |||||||
chr4:153535737 | A | C | 1 | a0001c0005t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.240-14336A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535737 | |||||||
chr4:153535774 | A | G | 1 | a0001c0002t0001g0091 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.240-14299A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535774 | |||||||
chr4:153535821 | A | G | 1 | a0001c0037t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.240-14252A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535821 | |||||||
chr4:153535823 | T | C | 3 | a0001c0001t0001g0244 a0001c0008t0001g0204 a0001c0021t0001g0014 |
3 | HG02145.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.240-14250T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535823 | |||||||
chr4:153535849 | T | A | 24 | a0001c0002t0001g0024 a0001c0003t0001g0141 a0001c0003t0001g0239 others(21): Show |
24 | HG00140.hp1 HG00609.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.240-14224T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535849 | |||||||
chr4:153535914 | C | T | 1 | a0001c0021t0001g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.240-14159C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153535914 | |||||||
chr4:153536170 | A | T | 5 | a0001c0001t0001g0086 a0001c0005t0001g0218 a0001c0037t0001g0230 others(2): Show |
5 | HG02055.hp1 HG02615.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-13903A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536170 | |||||||
chr4:153536176 | G | A | 24 | a0001c0003t0001g0141 a0001c0003t0001g0239 a0001c0004t0001g0125 others(21): Show |
24 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.240-13897G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536176 | |||||||
chr4:153536239 | G | C | 2 | a0001c0003t0001g0122 a0001c0003t0001g0196 |
2 | HG00735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-13834G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536239 | |||||||
chr4:153536306 | A | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.240-13767A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536306 | |||||||
chr4:153536367 | G | A | 26 | a0001c0001t0001g0237 a0001c0003t0001g0141 a0001c0003t0001g0239 others(23): Show |
26 | HG00140.hp1 HG00609.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.240-13706G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536367 | |||||||
chr4:153536464 | C | T | 1 | a0001c0005t0003g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.240-13609C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536464 | |||||||
chr4:153536553 | GAAAC | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.240-13518_240-1351 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153536553 | ||||||
chr4:153536681 | A | G | 1 | a0001c0002t0001g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.240-13392A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536681 | |||||||
chr4:153536718 | A | C | 1 | a0002c0006t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.240-13355A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536718 | |||||||
chr4:153536718 | ATCTC | A | 23 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(20): Show |
23 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.240-13354_240-1335 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536718 | |||||||
chr4:153536719 | T | C | 1 | a0002c0006t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.240-13354T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536719 | |||||||
chr4:153536866 | T | G | 1 | a0001c0004t0001g0212 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.240-13207T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536866 | |||||||
chr4:153536903 | C | T | 23 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(20): Show |
23 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.240-13170C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536903 | |||||||
chr4:153536916 | A | G | 106 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0086 others(103): Show |
106 | HG00140.hp1 HG00609.hp1 HG01081.hp1 others(103): Show |
intron_variant | MODIFIER | c.240-13157A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153536916 | |||||||
chr4:153537014 | G | A | 3 | a0001c0001t0001g0097 a0002c0007t0001g0096 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.240-13059G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537014 | |||||||
chr4:153537026 | T | A | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-13047T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537026 | |||||||
chr4:153537237 | A | G | 1 | a0001c0002t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.240-12836A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537237 | |||||||
chr4:153537274 | G | C | 6 | a0001c0012t0001g0131 a0001c0013t0001g0049 a0001c0013t0001g0088 others(3): Show |
6 | HG03654.hp1 HG04199.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-12799G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537274 | |||||||
chr4:153537284 | A | C | 2 | a0001c0005t0001g0238 a0004c0018t0001g0029 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.240-12789A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537284 | |||||||
chr4:153537319 | AAG | A | 23 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(20): Show |
23 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.240-12747_240-1274 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153537319 | ||||||
chr4:153537532 | G | A | 32 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(29): Show |
32 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.240-12541G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537532 | |||||||
chr4:153537534 | A | G | 1 | a0010c0038t0001g0056 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.240-12539A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537534 | |||||||
chr4:153537592 | T | C | 37 | a0001c0001t0001g0086 a0001c0001t0001g0223 a0001c0001t0001g0224 others(34): Show |
37 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.240-12481T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537592 | |||||||
chr4:153537651 | G | A | 11 | a0001c0001t0001g0086 a0001c0005t0001g0218 a0001c0012t0001g0131 others(8): Show |
11 | HG02055.hp1 HG02615.hp2 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.240-12422G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537651 | |||||||
chr4:153537788 | T | C | 1 | a0001c0002t0001g0213 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.240-12285T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537788 | |||||||
chr4:153537889 | G | T | 2 | a0001c0005t0001g0238 a0004c0018t0001g0029 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.240-12184G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537889 | |||||||
chr4:153537948 | T | C | 1 | a0001c0021t0001g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.240-12125T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537948 | |||||||
chr4:153537988 | A | G | 1 | a0001c0004t0001g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.240-12085A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153537988 | |||||||
chr4:153538405 | G | A | 1 | a0001c0005t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.240-11668G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538405 | |||||||
chr4:153538553 | C | CT | 21 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(18): Show |
21 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-11517dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153538553 | ||||||
chr4:153538586 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.240-11487C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538586 | |||||||
chr4:153538686 | T | C | 109 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0086 others(106): Show |
109 | HG00140.hp1 HG00609.hp1 HG01081.hp1 others(106): Show |
intron_variant | MODIFIER | c.240-11387T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538686 | |||||||
chr4:153538749 | T | A | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240-11324T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538749 | |||||||
chr4:153538803 | G | C | 22 | a0001c0003t0001g0141 a0001c0003t0001g0239 a0001c0004t0001g0125 others(19): Show |
22 | HG00140.hp1 HG00609.hp1 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.240-11270G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538803 | |||||||
chr4:153538806 | C | G | 21 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(18): Show |
21 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-11267C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538806 | |||||||
chr4:153538919 | C | CT | 21 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(18): Show |
21 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-11154_240-1115 others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538919 | |||||||
chr4:153538957 | C | T | 2 | a0001c0005t0001g0238 a0004c0018t0001g0029 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.240-11116C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538957 | |||||||
chr4:153538959 | C | T | 23 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(20): Show |
23 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.240-11114C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538959 | |||||||
chr4:153538972 | A | G | 1 | a0001c0037t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.240-11101A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153538972 | |||||||
chr4:153539093 | G | A | 22 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(19): Show |
22 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.240-10980G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539093 | |||||||
chr4:153539139 | A | C | 4 | a0001c0005t0001g0218 a0001c0037t0001g0230 a0004c0027t0001g0248 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-10934A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539139 | |||||||
chr4:153539263 | G | A | 21 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(18): Show |
21 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-10810G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539263 | |||||||
chr4:153539319 | A | G | 21 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(18): Show |
21 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-10754A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539319 | |||||||
chr4:153539492 | A | AT | 11 | a0001c0001t0001g0008 a0001c0002t0001g0051 a0001c0002t0001g0057 others(8): Show |
11 | HG01346.hp2 HG01928.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.240-10555dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153539492 | ||||||
chr4:153539492 | A | ATT | 5 | a0001c0024t0001g0010 a0001c0034t0001g0020 a0002c0010t0001g0021 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-10556_240-1055 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153539492 | ||||||
chr4:153539492 | AT | A | 26 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0219 others(23): Show |
26 | HG01099.hp2 HG01516.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.240-10555delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153539492 | ||||||
chr4:153539492 | ATT | A | 5 | a0001c0002t0001g0076 a0001c0005t0001g0218 a0001c0005t0001g0221 others(2): Show |
5 | HG02055.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-10556_240-1055 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153539492 | ||||||
chr4:153539492 | ATTT | A | 10 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(7): Show |
10 | HG02257.hp1 HG02647.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.240-10557_240-1055 others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153539492 | ||||||
chr4:153539492 | ATTTTT | A | 23 | a0001c0002t0001g0009 a0001c0003t0001g0141 a0001c0003t0001g0239 others(20): Show |
23 | HG00140.hp1 HG00609.hp1 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.240-10559_240-1055 others(9): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153539492 | ||||||
chr4:153539561 | G | A | 9 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.240-10512G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539561 | |||||||
chr4:153539651 | G | C | 1 | a0001c0008t0001g0187 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.240-10422G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539651 | |||||||
chr4:153539656 | A | G | 148 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(145): Show |
148 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.240-10417A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539656 | |||||||
chr4:153539665 | T | C | 3 | a0001c0005t0001g0218 a0001c0037t0001g0230 a0004c0027t0001g0248 |
3 | HG02055.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.240-10408T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539665 | |||||||
chr4:153539705 | A | G | 2 | a0001c0014t0001g0211 a0002c0010t0001g0069 |
2 | HG00558.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.240-10368A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539705 | |||||||
chr4:153539808 | T | A | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.240-10265T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539808 | |||||||
chr4:153539808 | T | TA | 111 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(108): Show |
111 | HG00140.hp1 HG00609.hp1 HG01081.hp1 others(108): Show |
intron_variant | MODIFIER | c.240-10255dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153539808 | ||||||
chr4:153539849 | G | A | 2 | a0001c0013t0001g0090 a0011c0035t0001g0035 |
2 | HG02615.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.240-10224G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539849 | |||||||
chr4:153539930 | G | A | 1 | a0001c0004t0001g0212 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.240-10143G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539930 | |||||||
chr4:153539930 | G | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0089 others(47): Show |
50 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.240-10143G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153539930 | |||||||
chr4:153540007 | A | G | 1 | a0001c0004t0001g0212 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.240-10066A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540007 | |||||||
chr4:153540131 | CA | C | 112 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(109): Show |
112 | HG00140.hp1 HG00609.hp1 HG01081.hp1 others(109): Show |
intron_variant | MODIFIER | c.240-9931delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153540131 | ||||||
chr4:153540142 | A | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(35): Show |
38 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.240-9931A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540142 | |||||||
chr4:153540161 | C | CT | 22 | a0001c0003t0001g0141 a0001c0003t0001g0239 a0001c0004t0001g0125 others(19): Show |
22 | HG00140.hp1 HG00609.hp1 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.240-9911dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153540161 | ||||||
chr4:153540201 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.240-9872C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540201 | |||||||
chr4:153540345 | T | A | 1 | a0002c0031t0001g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.240-9728T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540345 | |||||||
chr4:153540436 | C | T | 1 | a0001c0005t0003g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.240-9637C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540436 | |||||||
chr4:153540612 | G | C | 1 | a0001c0011t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.240-9461G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540612 | |||||||
chr4:153540732 | T | G | 113 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(110): Show |
113 | HG00140.hp1 HG00609.hp1 HG01081.hp1 others(110): Show |
intron_variant | MODIFIER | c.240-9341T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540732 | |||||||
chr4:153540780 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(110): Show |
113 | HG00140.hp1 HG00609.hp1 HG01081.hp1 others(110): Show |
intron_variant | MODIFIER | c.240-9293G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540780 | |||||||
chr4:153540978 | C | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0095 others(35): Show |
38 | HG01081.hp1 HG01123.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.240-9095C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153540978 | |||||||
chr4:153541018 | T | C | 1 | a0001c0014t0001g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.240-9055T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153541018 | |||||||
chr4:153541103 | T | A | 2 | a0001c0005t0001g0238 a0004c0018t0001g0029 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.240-8970T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153541103 | |||||||
chr4:153541562 | G | A | 2 | a0002c0010t0001g0073 a0002c0010t0001g0075 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.240-8511G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153541562 | |||||||
chr4:153541698 | G | T | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-8375G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153541698 | |||||||
chr4:153541772 | A | G | 8 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(5): Show |
8 | HG02257.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.240-8301A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153541772 | |||||||
chr4:153541871 | G | C | 8 | a0001c0001t0001g0097 a0001c0003t0001g0124 a0002c0007t0001g0070 others(5): Show |
8 | HG01099.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-8202G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153541871 | |||||||
chr4:153541897 | C | T | 35 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0223 others(32): Show |
35 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.240-8176C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153541897 | |||||||
chr4:153541924 | TG | T | 13 | a0001c0001t0001g0089 a0001c0002t0001g0092 a0001c0011t0001g0048 others(10): Show |
13 | HG03654.hp1 HG03831.hp1 HG04199.hp1 others(10): Show |
intron_variant | MODIFIER | c.240-8148delG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153541924 | |||||||
chr4:153542002 | G | A | 48 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0089 others(45): Show |
48 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(45): Show |
intron_variant | MODIFIER | c.240-8071G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542002 | |||||||
chr4:153542009 | C | T | 2 | a0001c0002t0001g0100 a0001c0033t0001g0099 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-8064C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542009 | |||||||
chr4:153542166 | C | T | 13 | a0001c0001t0001g0089 a0001c0002t0001g0092 a0001c0011t0001g0048 others(10): Show |
13 | HG03654.hp1 HG03831.hp1 HG04199.hp1 others(10): Show |
intron_variant | MODIFIER | c.240-7907C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542166 | |||||||
chr4:153542188 | G | A | 1 | a0001c0004t0001g0142 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.240-7885G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542188 | |||||||
chr4:153542208 | G | A | 1 | a0001c0047t0001g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.240-7865G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542208 | |||||||
chr4:153542225 | A | C | 1 | a0001c0002t0001g0217 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.240-7848A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542225 | |||||||
chr4:153542239 | TAGAA | T | 13 | a0001c0001t0001g0089 a0001c0002t0001g0092 a0001c0011t0001g0048 others(10): Show |
13 | HG03654.hp1 HG03831.hp1 HG04199.hp1 others(10): Show |
intron_variant | MODIFIER | c.240-7831_240-7828d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153542239 | ||||||
chr4:153542399 | C | CGTT | 116 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(113): Show |
116 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.240-7672_240-7670d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153542399 | ||||||
chr4:153542468 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.240-7605C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542468 | |||||||
chr4:153542549 | A | C | 1 | a0002c0016t0001g0191 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.240-7524A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542549 | |||||||
chr4:153542556 | A | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0089 others(65): Show |
68 | HG00140.hp1 HG00609.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.240-7517A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542556 | |||||||
chr4:153542630 | T | C | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.240-7443T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542630 | |||||||
chr4:153542691 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0086 others(56): Show |
59 | HG00558.hp1 HG01243.hp2 HG01884.hp2 others(56): Show |
intron_variant | MODIFIER | c.240-7382A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542691 | |||||||
chr4:153542941 | A | G | 15 | a0001c0001t0001g0089 a0001c0002t0001g0047 a0001c0002t0001g0092 others(12): Show |
15 | HG03654.hp1 HG03654.hp2 HG03831.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-7132A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153542941 | |||||||
chr4:153543021 | G | C | 107 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(104): Show |
107 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.240-7052G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153543021 | |||||||
chr4:153543041 | C | T | 15 | a0001c0001t0001g0089 a0001c0002t0001g0047 a0001c0002t0001g0092 others(12): Show |
15 | HG03654.hp1 HG03654.hp2 HG03831.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-7032C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153543041 | |||||||
chr4:153543180 | T | C | 32 | a0001c0001t0001g0012 a0001c0001t0001g0219 a0001c0001t0001g0222 others(29): Show |
32 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.240-6893T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153543180 | |||||||
chr4:153543221 | G | C | 1 | a0004c0018t0001g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.240-6852G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153543221 | |||||||
chr4:153543581 | G | A | 2 | a0002c0006t0001g0132 a0002c0010t0001g0085 |
2 | HG00609.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.240-6492G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153543581 | |||||||
chr4:153543825 | G | A | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.240-6248G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153543825 | |||||||
chr4:153544306 | A | ACAG | 5 | a0001c0005t0001g0022 a0002c0010t0001g0021 a0002c0010t0001g0028 others(2): Show |
5 | HG02109.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.240-5766_240-5764d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153544306 | ||||||
chr4:153544370 | C | T | 4 | a0001c0001t0001g0237 a0001c0005t0001g0106 a0001c0028t0001g0108 others(1): Show |
4 | HG01884.hp2 HG02148.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-5703C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153544370 | |||||||
chr4:153544422 | G | A | 28 | a0001c0001t0001g0012 a0001c0001t0001g0219 a0001c0001t0001g0222 others(25): Show |
28 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.240-5651G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153544422 | |||||||
chr4:153544740 | C | T | 97 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0039 others(94): Show |
97 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.240-5333C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153544740 | |||||||
chr4:153544842 | G | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(101): Show |
104 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.240-5231G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153544842 | |||||||
chr4:153545051 | T | C | 1 | a0002c0006t0001g0132 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.240-5022T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545051 | |||||||
chr4:153545185 | G | T | 4 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG02622.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-4888G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545185 | |||||||
chr4:153545290 | C | CTT | 53 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0223 others(50): Show |
53 | HG00597.hp1 HG01081.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.240-4769_240-4768d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545290 | C | CTTTTTT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(36): Show |
39 | HG00597.hp2 HG01257.hp1 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.240-4773_240-4768d others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545290 | C | CTTTTTTT others(9): Show |
1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.240-4768_240-4767i others(18): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545290 | C | CTTTTTTT others(11): Show |
11 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0004t0001g0125 others(8): Show |
11 | HG00140.hp1 HG00609.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.240-4768_240-4767i others(20): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545290 | C | CTTTTTTT others(12): Show |
8 | a0001c0001t0002g0061 a0001c0001t0002g0082 a0001c0004t0001g0148 others(5): Show |
8 | HG02135.hp2 HG02257.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.240-4768_240-4767i others(21): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545290 | C | CTTTTTTT others(13): Show |
6 | a0001c0003t0001g0141 a0001c0004t0001g0171 a0001c0004t0001g0212 others(3): Show |
6 | HG00609.hp2 HG02135.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.240-4768_240-4767i others(22): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545290 | C | CTTTTTTT others(14): Show |
2 | a0001c0003t0001g0239 a0002c0006t0001g0200 |
2 | HG02071.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.240-4768_240-4767i others(23): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545290 | C | CTTTTTTT others(16): Show |
1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-4768_240-4767i others(25): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545290 | C | CTTTTTTT others(20): Show |
1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-4768_240-4767i others(29): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153545290 | ||||||
chr4:153545405 | A | G | 4 | a0001c0001t0001g0237 a0001c0005t0001g0106 a0001c0028t0001g0108 others(1): Show |
4 | HG01884.hp2 HG02148.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-4668A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545405 | |||||||
chr4:153545425 | C | G | 1 | a0001c0002t0001g0091 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.240-4648C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545425 | |||||||
chr4:153545677 | G | T | 1 | a0001c0011t0001g0050 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.240-4396G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545677 | |||||||
chr4:153545705 | T | C | 1 | a0006c0050t0001g0116 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.240-4368T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545705 | |||||||
chr4:153545787 | C | T | 151 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(148): Show |
151 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.240-4286C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545787 | |||||||
chr4:153545894 | T | C | 1 | a0001c0009t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.240-4179T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545894 | |||||||
chr4:153545943 | G | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
71 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.240-4130G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545943 | |||||||
chr4:153545947 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.240-4126G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153545947 | |||||||
chr4:153546044 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(70): Show |
73 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.240-4029G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546044 | |||||||
chr4:153546057 | G | GTT | 17 | a0001c0001t0001g0089 a0001c0002t0001g0047 a0001c0002t0001g0092 others(14): Show |
17 | HG02523.hp1 HG03654.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.240-4015_240-4014d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153546057 | ||||||
chr4:153546130 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.240-3943A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546130 | |||||||
chr4:153546214 | C | CT | 27 | a0001c0001t0001g0089 a0001c0002t0001g0047 a0001c0002t0001g0092 others(24): Show |
27 | HG02055.hp1 HG02523.hp1 HG02615.hp2 others(24): Show |
intron_variant | MODIFIER | c.240-3844dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153546214 | ||||||
chr4:153546214 | C | CTT | 6 | a0001c0002t0001g0100 a0001c0008t0001g0187 a0001c0009t0001g0177 others(3): Show |
6 | HG02293.hp1 HG03579.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-3845_240-3844d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153546214 | ||||||
chr4:153546214 | CT | C | 15 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(12): Show |
15 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.240-3844delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153546214 | ||||||
chr4:153546270 | T | C | 1 | a0004c0018t0001g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.240-3803T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546270 | |||||||
chr4:153546273 | G | A | 2 | a0001c0002t0001g0100 a0004c0027t0001g0248 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.240-3800G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546273 | |||||||
chr4:153546305 | T | C | 17 | a0001c0001t0001g0089 a0001c0002t0001g0047 a0001c0002t0001g0092 others(14): Show |
17 | HG02523.hp1 HG03654.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.240-3768T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546305 | |||||||
chr4:153546333 | G | A | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.240-3740G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546333 | |||||||
chr4:153546529 | A | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(47): Show |
50 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(47): Show |
intron_variant | MODIFIER | c.240-3544A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546529 | |||||||
chr4:153546693 | C | T | 2 | a0001c0009t0001g0175 a0002c0006t0001g0210 |
2 | NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.240-3380C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546693 | |||||||
chr4:153546881 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(74): Show |
77 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.240-3192C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546881 | |||||||
chr4:153546938 | A | G | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.240-3135A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153546938 | |||||||
chr4:153547018 | C | T | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-3055C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547018 | |||||||
chr4:153547119 | T | C | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240-2954T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547119 | |||||||
chr4:153547130 | A | T | 21 | a0001c0003t0001g0141 a0001c0003t0001g0239 a0001c0004t0001g0125 others(18): Show |
21 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.240-2943A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547130 | |||||||
chr4:153547137 | T | C | 3 | a0001c0002t0001g0100 a0001c0005t0001g0238 a0004c0027t0001g0248 |
3 | HG02717.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.240-2936T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547137 | |||||||
chr4:153547145 | A | G | 54 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0086 others(51): Show |
54 | HG00597.hp1 HG01081.hp1 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.240-2928A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547145 | |||||||
chr4:153547268 | T | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(76): Show |
79 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.240-2805T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547268 | |||||||
chr4:153547330 | A | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(153): Show |
156 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.240-2743A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547330 | |||||||
chr4:153547413 | T | C | 1 | a0002c0043t0001g0209 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.240-2660T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547413 | |||||||
chr4:153547496 | G | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(95): Show |
98 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.240-2577G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547496 | |||||||
chr4:153547530 | A | G | 1 | a0004c0018t0001g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.240-2543A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547530 | |||||||
chr4:153547610 | A | G | 2 | a0001c0002t0001g0100 a0004c0027t0001g0248 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.240-2463A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547610 | |||||||
chr4:153547687 | C | G | 97 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(94): Show |
97 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.240-2386C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547687 | |||||||
chr4:153547731 | T | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(154): Show |
157 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.240-2342T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153547731 | |||||||
chr4:153548011 | G | C | 1 | a0004c0018t0001g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.240-2062G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548011 | |||||||
chr4:153548027 | T | TC | 94 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(91): Show |
94 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.240-2046_240-2045i others(3): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548027 | |||||||
chr4:153548062 | G | A | 55 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0086 others(52): Show |
55 | HG00597.hp1 HG01081.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.240-2011G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548062 | |||||||
chr4:153548113 | C | T | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.240-1960C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548113 | |||||||
chr4:153548136 | G | A | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240-1937G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548136 | |||||||
chr4:153548174 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0244 a0001c0008t0001g0204 others(1): Show |
4 | HG02145.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-1899G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548174 | |||||||
chr4:153548175 | G | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(149): Show |
152 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.240-1898G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548175 | |||||||
chr4:153548183 | C | T | 2 | a0001c0005t0001g0218 a0011c0035t0001g0035 |
2 | HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.240-1890C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548183 | |||||||
chr4:153548305 | CTTTTTAT others(3): Show |
C | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240-1764_240-1755d others(12): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153548305 | ||||||
chr4:153548472 | T | C | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-1601T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548472 | |||||||
chr4:153548473 | T | A | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240-1600T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548473 | |||||||
chr4:153548521 | C | T | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240-1552C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548521 | |||||||
chr4:153548549 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0222 others(6): Show |
9 | HG01891.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.240-1524C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548549 | |||||||
chr4:153548555 | A | G | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240-1518A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548555 | |||||||
chr4:153548747 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.240-1326T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548747 | |||||||
chr4:153548932 | G | A | 1 | a0001c0005t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.240-1141G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548932 | |||||||
chr4:153548963 | T | C | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.240-1110T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153548963 | |||||||
chr4:153549227 | A | G | 1 | a0002c0006t0001g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.240-846A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549227 | |||||||
chr4:153549243 | A | G | 1 | a0002c0015t0001g0018 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.240-830A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549243 | |||||||
chr4:153549370 | T | C | 1 | a0002c0016t0001g0191 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.240-703T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549370 | |||||||
chr4:153549551 | A | G | 5 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0007 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-522A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549551 | |||||||
chr4:153549561 | A | T | 1 | a0001c0005t0001g0247 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.240-512A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549561 | |||||||
chr4:153549603 | G | C | 159 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(156): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.240-470G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549603 | |||||||
chr4:153549607 | A | G | 51 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(48): Show |
51 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(48): Show |
intron_variant | MODIFIER | c.240-466A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549607 | |||||||
chr4:153549710 | A | G | 2 | a0002c0010t0001g0073 a0002c0010t0001g0075 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.240-363A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549710 | |||||||
chr4:153549873 | A | G | 1 | a0001c0005t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.240-200A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549873 | |||||||
chr4:153549961 | G | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(154): Show |
157 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.240-112G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549961 | |||||||
chr4:153549984 | G | T | 1 | a0001c0002t0001g0100 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.240-89G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153549984 | |||||||
chr4:153550009 | C | T | 14 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0006 others(11): Show |
14 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.240-64C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | chr4 | 153550009 | |||||||
chr4:153550053 | CCT | C | 3 | a0001c0009t0001g0104 a0002c0025t0001g0103 a0002c0051t0001g0102 |
3 | NA18943.hp1 NA18950.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.240-15_240-14delCT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr4 | 153550053 | ||||||
chr4:153550396 | T | G | 1 | a0001c0026t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.308+255T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550396 | |||||||
chr4:153550432 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.308+291T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550432 | |||||||
chr4:153550464 | C | T | 4 | a0001c0004t0001g0127 a0003c0019t0001g0154 a0003c0019t0001g0198 others(1): Show |
4 | HG01928.hp2 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+323C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550464 | |||||||
chr4:153550475 | C | A | 38 | a0001c0001t0001g0042 a0001c0001t0001g0086 a0001c0002t0001g0002 others(35): Show |
38 | HG00597.hp1 HG01081.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.308+334C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550475 | |||||||
chr4:153550484 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0244 a0001c0008t0001g0204 others(1): Show |
4 | HG02145.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+343G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550484 | |||||||
chr4:153550487 | C | T | 1 | a0001c0011t0001g0112 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.308+346C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550487 | |||||||
chr4:153550493 | A | AT | 3 | a0001c0026t0001g0077 a0002c0006t0001g0118 a0002c0016t0001g0139 |
3 | HG00558.hp1 HG02523.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.308+358dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr4 | 153550493 | ||||||
chr4:153550528 | G | A | 2 | a0001c0037t0001g0230 a0004c0018t0001g0029 |
2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.308+387G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550528 | |||||||
chr4:153550533 | C | T | 1 | a0001c0004t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.308+392C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550533 | |||||||
chr4:153550534 | G | T | 1 | a0001c0002t0001g0217 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.308+393G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550534 | |||||||
chr4:153550559 | T | C | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.308+418T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550559 | |||||||
chr4:153550607 | C | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(150): Show |
153 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.308+466C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550607 | |||||||
chr4:153550616 | A | G | 4 | a0001c0001t0001g0237 a0001c0005t0001g0106 a0001c0028t0001g0108 others(1): Show |
4 | HG01884.hp2 HG02148.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+475A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550616 | |||||||
chr4:153550618 | T | G | 4 | a0001c0001t0001g0237 a0001c0005t0001g0106 a0001c0028t0001g0108 others(1): Show |
4 | HG01884.hp2 HG02148.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+477T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550618 | |||||||
chr4:153550621 | T | C | 4 | a0001c0001t0001g0237 a0001c0005t0001g0106 a0001c0028t0001g0108 others(1): Show |
4 | HG01884.hp2 HG02148.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+480T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550621 | |||||||
chr4:153550659 | T | G | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.308+518T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550659 | |||||||
chr4:153550681 | T | TAAG | 159 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(156): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.308+541_308+543dup others(3): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr4 | 153550681 | ||||||
chr4:153550688 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.308+547A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550688 | |||||||
chr4:153550712 | G | A | 18 | a0001c0002t0001g0002 a0001c0002t0001g0045 a0001c0003t0001g0133 others(15): Show |
18 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.308+571G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550712 | |||||||
chr4:153550731 | A | ACT | 159 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(156): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.308+591_308+592dup others(2): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr4 | 153550731 | ||||||
chr4:153550776 | G | A | 159 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(156): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.308+635G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550776 | |||||||
chr4:153550810 | G | C | 1 | a0014c0042t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.308+669G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153550810 | |||||||
chr4:153551230 | C | T | 9 | a0001c0001t0001g0039 a0001c0005t0001g0022 a0001c0005t0001g0221 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.308+1089C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551230 | |||||||
chr4:153551359 | ATT | A | 151 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(148): Show |
151 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.308+1233_308+1234d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr4 | 153551359 | ||||||
chr4:153551425 | T | G | 33 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0089 others(30): Show |
33 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.308+1284T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551425 | |||||||
chr4:153551426 | C | T | 33 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0089 others(30): Show |
33 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.308+1285C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551426 | |||||||
chr4:153551444 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.308+1303G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551444 | |||||||
chr4:153551460 | C | T | 7 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.308+1319C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551460 | |||||||
chr4:153551497 | A | G | 1 | a0004c0027t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.308+1356A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551497 | |||||||
chr4:153551514 | C | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(150): Show |
153 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.308+1373C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551514 | |||||||
chr4:153551567 | G | T | 144 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(141): Show |
144 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.308+1426G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551567 | |||||||
chr4:153551699 | A | G | 2 | a0001c0001t0001g0219 a0014c0042t0001g0001 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.308+1558A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551699 | |||||||
chr4:153551736 | G | C | 80 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(77): Show |
80 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.308+1595G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551736 | |||||||
chr4:153551926 | A | T | 4 | a0001c0001t0001g0237 a0001c0005t0001g0106 a0001c0028t0001g0108 others(1): Show |
4 | HG01884.hp2 HG02148.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+1785A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551926 | |||||||
chr4:153551934 | C | T | 51 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(48): Show |
51 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(48): Show |
intron_variant | MODIFIER | c.308+1793C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153551934 | |||||||
chr4:153552037 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(150): Show |
153 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.308+1896G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552037 | |||||||
chr4:153552055 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.308+1914C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552055 | |||||||
chr4:153552108 | G | A | 1 | a0002c0031t0001g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.308+1967G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552108 | |||||||
chr4:153552149 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.308+2008G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552149 | |||||||
chr4:153552183 | A | T | 3 | a0001c0001t0001g0244 a0001c0008t0001g0204 a0001c0021t0001g0014 |
3 | HG02145.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.308+2042A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552183 | |||||||
chr4:153552425 | T | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(141): Show |
144 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.308+2284T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552425 | |||||||
chr4:153552624 | A | G | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.308+2483A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552624 | |||||||
chr4:153552658 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.308+2517C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552658 | |||||||
chr4:153552678 | T | C | 1 | a0001c0002t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.308+2537T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552678 | |||||||
chr4:153552679 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.308+2538T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552679 | |||||||
chr4:153552803 | C | T | 1 | a0002c0006t0001g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.308+2662C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552803 | |||||||
chr4:153552880 | T | C | 1 | a0001c0012t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.308+2739T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552880 | |||||||
chr4:153552930 | G | A | 149 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(146): Show |
149 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.308+2789G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552930 | |||||||
chr4:153552944 | TG | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(106): Show |
109 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.308+2804delG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552944 | |||||||
chr4:153552945 | G | T | 35 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0089 others(32): Show |
35 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.308+2804G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552945 | |||||||
chr4:153552956 | T | C | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.308+2815T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552956 | |||||||
chr4:153552960 | T | G | 1 | a0001c0011t0001g0050 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.308+2819T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153552960 | |||||||
chr4:153553023 | A | G | 17 | a0001c0001t0001g0089 a0001c0002t0001g0047 a0001c0002t0001g0092 others(14): Show |
17 | HG02523.hp1 HG03654.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.309-2764A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553023 | |||||||
chr4:153553098 | A | G | 41 | a0001c0001t0001g0042 a0001c0001t0001g0223 a0001c0001t0001g0224 others(38): Show |
41 | HG00597.hp1 HG01081.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.309-2689A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553098 | |||||||
chr4:153553113 | T | A | 41 | a0001c0001t0001g0042 a0001c0001t0001g0223 a0001c0001t0001g0224 others(38): Show |
41 | HG00597.hp1 HG01081.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.309-2674T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553113 | |||||||
chr4:153553143 | C | T | 3 | a0001c0001t0001g0039 a0001c0002t0001g0009 a0011c0035t0001g0035 |
3 | HG01243.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.309-2644C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553143 | |||||||
chr4:153553152 | G | A | 8 | a0001c0005t0001g0022 a0001c0005t0001g0221 a0001c0024t0001g0010 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.309-2635G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553152 | |||||||
chr4:153553188 | A | C | 30 | a0001c0001t0001g0042 a0001c0002t0001g0002 a0001c0002t0001g0005 others(27): Show |
30 | HG00597.hp1 HG01081.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.309-2599A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553188 | |||||||
chr4:153553195 | T | C | 3 | a0001c0001t0001g0039 a0001c0002t0001g0009 a0011c0035t0001g0035 |
3 | HG01243.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.309-2592T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553195 | |||||||
chr4:153553287 | C | T | 2 | a0001c0003t0001g0172 a0001c0003t0001g0173 |
2 | NA18981.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.309-2500C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553287 | |||||||
chr4:153553392 | A | T | 29 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0089 others(26): Show |
29 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.309-2395A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553392 | |||||||
chr4:153553457 | T | TA | 87 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(84): Show |
87 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.309-2316dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr4 | 153553457 | ||||||
chr4:153553457 | T | TAAA | 7 | a0001c0005t0001g0022 a0001c0005t0001g0221 a0001c0024t0001g0010 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-2318_309-2316d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr4 | 153553457 | ||||||
chr4:153553587 | TCTC | T | 12 | a0001c0002t0001g0051 a0001c0002t0001g0054 a0001c0002t0001g0057 others(9): Show |
12 | HG00544.hp1 HG02071.hp1 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.309-2194_309-2192d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr4 | 153553587 | ||||||
chr4:153553615 | T | A | 18 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0002t0001g0047 others(15): Show |
18 | HG02523.hp1 HG03654.hp1 HG03654.hp2 others(15): Show |
intron_variant | MODIFIER | c.309-2172T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553615 | |||||||
chr4:153553628 | A | G | 1 | a0001c0014t0001g0138 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.309-2159A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553628 | |||||||
chr4:153553651 | C | G | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.309-2136C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553651 | |||||||
chr4:153553665 | C | T | 2 | a0001c0001t0001g0219 a0014c0042t0001g0001 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.309-2122C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553665 | |||||||
chr4:153553720 | C | T | 144 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(141): Show |
144 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.309-2067C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553720 | |||||||
chr4:153553779 | G | A | 145 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(142): Show |
145 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.309-2008G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553779 | |||||||
chr4:153553784 | A | G | 1 | a0001c0013t0001g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.309-2003A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553784 | |||||||
chr4:153553814 | A | G | 3 | a0001c0001t0001g0244 a0001c0008t0001g0204 a0001c0021t0001g0014 |
3 | HG02145.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.309-1973A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553814 | |||||||
chr4:153553844 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.309-1943G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553844 | |||||||
chr4:153553919 | A | T | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-1868A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153553919 | |||||||
chr4:153554045 | C | T | 1 | a0002c0006t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.309-1742C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554045 | |||||||
chr4:153554065 | T | C | 8 | a0001c0005t0001g0022 a0001c0005t0001g0221 a0001c0024t0001g0010 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.309-1722T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554065 | |||||||
chr4:153554136 | T | C | 8 | a0001c0005t0001g0022 a0001c0005t0001g0221 a0001c0024t0001g0010 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.309-1651T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554136 | |||||||
chr4:153554167 | A | G | 3 | a0001c0001t0001g0244 a0001c0008t0001g0204 a0001c0021t0001g0014 |
3 | HG02145.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.309-1620A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554167 | |||||||
chr4:153554218 | C | A | 1 | a0001c0033t0001g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.309-1569C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554218 | |||||||
chr4:153554254 | C | G | 1 | a0002c0045t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.309-1533C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554254 | |||||||
chr4:153554286 | A | T | 2 | a0001c0005t0001g0238 a0004c0027t0001g0248 |
2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.309-1501A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554286 | |||||||
chr4:153554399 | A | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(141): Show |
144 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.309-1388A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554399 | |||||||
chr4:153554519 | G | A | 144 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(141): Show |
144 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.309-1268G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554519 | |||||||
chr4:153554664 | A | G | 2 | a0001c0005t0001g0238 a0004c0027t0001g0248 |
2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.309-1123A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554664 | |||||||
chr4:153554851 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.309-936G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554851 | |||||||
chr4:153554918 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(123): Show |
126 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.309-869C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153554918 | |||||||
chr4:153555125 | G | A | 8 | a0001c0005t0001g0022 a0001c0005t0001g0221 a0001c0024t0001g0010 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.309-662G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555125 | |||||||
chr4:153555219 | A | G | 1 | a0001c0004t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.309-568A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555219 | |||||||
chr4:153555234 | T | G | 17 | a0001c0001t0001g0089 a0001c0002t0001g0047 a0001c0002t0001g0092 others(14): Show |
17 | HG02523.hp1 HG03654.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.309-553T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555234 | |||||||
chr4:153555242 | C | T | 145 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(142): Show |
145 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.309-545C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555242 | |||||||
chr4:153555323 | A | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(33): Show |
36 | HG00544.hp2 HG00597.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.309-464A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555323 | |||||||
chr4:153555347 | G | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(145): Show |
148 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.309-440G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555347 | |||||||
chr4:153555364 | C | T | 1 | a0001c0012t0001g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.309-423C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555364 | |||||||
chr4:153555365 | G | A | 2 | a0001c0026t0001g0077 a0002c0016t0001g0139 |
2 | HG00558.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.309-422G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555365 | |||||||
chr4:153555548 | T | A | 1 | a0001c0008t0001g0199 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.309-239T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555548 | |||||||
chr4:153555723 | T | C | 5 | a0001c0005t0001g0022 a0002c0010t0001g0021 a0002c0010t0001g0028 others(2): Show |
5 | HG02109.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.309-64T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555723 | |||||||
chr4:153555724 | A | G | 2 | a0002c0057t0001g0032 a0013c0058t0001g0031 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.309-63A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555724 | |||||||
chr4:153555772 | T | C | 19 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0219 others(16): Show |
19 | HG00597.hp1 HG01081.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.309-15T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 4/34 | chr4 | 153555772 | |||||||
chr4:153555931 | G | A | 1 | a0001c0003t0001g0157 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.432+21G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153555931 | |||||||
chr4:153556127 | G | T | 2 | a0001c0001t0002g0082 a0001c0005t0001g0218 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.432+217G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556127 | |||||||
chr4:153556140 | A | G | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.432+230A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556140 | |||||||
chr4:153556277 | T | C | 6 | a0001c0005t0001g0022 a0001c0005t0001g0238 a0002c0010t0001g0021 others(3): Show |
6 | HG02109.hp2 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+367T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556277 | |||||||
chr4:153556317 | G | A | 1 | a0002c0010t0001g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.432+407G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556317 | |||||||
chr4:153556389 | C | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.432+479C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556389 | |||||||
chr4:153556489 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0219 a0001c0005t0001g0247 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-477A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556489 | |||||||
chr4:153556512 | TA | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(121): Show |
124 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.433-444delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr4 | 153556512 | ||||||
chr4:153556590 | G | A | 1 | a0001c0008t0001g0184 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.433-376G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556590 | |||||||
chr4:153556619 | A | G | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.433-347A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556619 | |||||||
chr4:153556620 | T | C | 5 | a0001c0005t0001g0022 a0002c0010t0001g0021 a0002c0010t0001g0028 others(2): Show |
5 | HG02109.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-346T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556620 | |||||||
chr4:153556643 | A | G | 15 | a0001c0001t0001g0244 a0001c0005t0001g0022 a0001c0005t0001g0218 others(12): Show |
15 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.433-323A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556643 | |||||||
chr4:153556658 | T | C | 2 | a0001c0024t0001g0015 a0001c0041t0001g0220 |
2 | HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.433-308T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556658 | |||||||
chr4:153556658 | T | G | 2 | a0001c0001t0001g0219 a0014c0042t0001g0001 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.433-308T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | chr4 | 153556658 | |||||||
chr4:153556848 | T | TAAATC | 136 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(133): Show |
136 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.433-116_433-115ins others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr4 | 153556848 | ||||||
chr4:153557148 | A | G | 34 | a0001c0001t0001g0219 a0001c0001t0002g0061 a0001c0001t0002g0062 others(31): Show |
34 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.549+66A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153557148 | |||||||
chr4:153557292 | A | G | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+210A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153557292 | |||||||
chr4:153557333 | A | C | 15 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0005t0001g0109 others(12): Show |
15 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.549+251A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153557333 | |||||||
chr4:153557456 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(93): Show |
96 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.549+374T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153557456 | |||||||
chr4:153557584 | C | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(100): Show |
103 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.549+502C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153557584 | |||||||
chr4:153557590 | A | G | 6 | a0001c0001t0001g0097 a0002c0006t0001g0202 a0002c0006t0001g0203 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.549+508A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153557590 | |||||||
chr4:153557734 | A | G | 6 | a0001c0001t0001g0097 a0002c0006t0001g0202 a0002c0006t0001g0203 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-524A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153557734 | |||||||
chr4:153557897 | A | G | 2 | a0001c0024t0001g0015 a0001c0041t0001g0220 |
2 | HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.550-361A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153557897 | |||||||
chr4:153558040 | G | A | 2 | a0001c0009t0001g0175 a0002c0006t0001g0210 |
2 | NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.550-218G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153558040 | |||||||
chr4:153558254 | G | A | 2 | a0001c0003t0001g0141 a0001c0012t0001g0169 |
2 | NA19074.hp2 NA19086.hp1 |
splice_region_variant&intron_variant | LOW | c.550-4G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 6/34 | chr4 | 153558254 | |||||||
chr4:153558420 | C | G | 6 | a0001c0001t0001g0097 a0002c0006t0001g0202 a0002c0006t0001g0203 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+52C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153558420 | |||||||
chr4:153558576 | T | G | 26 | a0001c0005t0001g0238 a0001c0009t0001g0177 a0001c0009t0001g0190 others(23): Show |
26 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.660+208T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153558576 | |||||||
chr4:153558617 | G | T | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.660+249G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153558617 | |||||||
chr4:153558982 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0002g0063 a0001c0033t0001g0099 |
3 | HG01243.hp2 HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.660+614A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153558982 | |||||||
chr4:153559017 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.660+649A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153559017 | |||||||
chr4:153559117 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.660+749C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153559117 | |||||||
chr4:153559189 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.660+821G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153559189 | |||||||
chr4:153559383 | C | G | 168 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(165): Show |
168 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.660+1015C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153559383 | |||||||
chr4:153559812 | T | C | 6 | a0001c0001t0001g0097 a0002c0006t0001g0202 a0002c0006t0001g0203 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1444T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153559812 | |||||||
chr4:153559860 | G | A | 3 | a0001c0002t0002g0065 a0001c0024t0001g0010 a0011c0035t0001g0035 |
3 | HG02280.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.660+1492G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153559860 | |||||||
chr4:153560136 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.660+1768C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153560136 | |||||||
chr4:153560240 | C | T | 1 | a0001c0021t0001g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.660+1872C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153560240 | |||||||
chr4:153560259 | G | A | 11 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(8): Show |
11 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.660+1891G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153560259 | |||||||
chr4:153560278 | A | G | 1 | a0001c0008t0001g0184 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.660+1910A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153560278 | |||||||
chr4:153560395 | T | C | 1 | a0001c0002t0001g0051 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.660+2027T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153560395 | |||||||
chr4:153560835 | A | G | 8 | a0001c0001t0001g0219 a0001c0005t0001g0022 a0001c0024t0001g0010 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+2467A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153560835 | |||||||
chr4:153560884 | T | A | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.660+2516T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153560884 | |||||||
chr4:153560926 | G | A | 2 | a0001c0024t0001g0015 a0001c0041t0001g0220 |
2 | HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.660+2558G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153560926 | |||||||
chr4:153561103 | T | C | 6 | a0001c0001t0001g0097 a0002c0006t0001g0202 a0002c0006t0001g0203 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+2735T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561103 | |||||||
chr4:153561106 | G | A | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.660+2738G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561106 | |||||||
chr4:153561336 | C | G | 1 | a0002c0016t0001g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.660+2968C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561336 | |||||||
chr4:153561500 | A | G | 3 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0081 |
3 | HG01891.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.660+3132A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561500 | |||||||
chr4:153561522 | C | G | 32 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0001t0001g0223 others(29): Show |
32 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+3154C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561522 | |||||||
chr4:153561629 | C | T | 2 | a0002c0057t0001g0032 a0013c0058t0001g0031 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.660+3261C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561629 | |||||||
chr4:153561696 | C | T | 18 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0005t0001g0022 others(15): Show |
18 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.660+3328C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561696 | |||||||
chr4:153561866 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.660+3498G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561866 | |||||||
chr4:153561949 | A | T | 2 | a0001c0011t0001g0048 a0001c0011t0001g0050 |
2 | HG03831.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.660+3581A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153561949 | |||||||
chr4:153561963 | C | CA | 71 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0059 others(68): Show |
71 | HG00558.hp1 HG00735.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.660+3607dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153561963 | ||||||
chr4:153561963 | C | CAA | 6 | a0001c0005t0001g0022 a0001c0009t0001g0170 a0002c0007t0001g0084 others(3): Show |
6 | HG02109.hp2 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+3606_660+3607d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153561963 | ||||||
chr4:153562041 | A | AT | 18 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0005t0001g0022 others(15): Show |
18 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.660+3687dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153562041 | ||||||
chr4:153562101 | G | A | 2 | a0001c0021t0001g0014 a0004c0018t0001g0029 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.660+3733G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562101 | |||||||
chr4:153562106 | C | T | 1 | a0001c0003t0001g0196 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.660+3738C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562106 | |||||||
chr4:153562123 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.660+3755C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562123 | |||||||
chr4:153562124 | G | A | 1 | a0002c0029t0001g0067 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.660+3756G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562124 | |||||||
chr4:153562287 | C | T | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.660+3919C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562287 | |||||||
chr4:153562299 | G | A | 1 | a0002c0043t0001g0209 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.660+3931G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562299 | |||||||
chr4:153562325 | C | T | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.660+3957C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562325 | |||||||
chr4:153562500 | A | G | 1 | a0001c0005t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.660+4132A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562500 | |||||||
chr4:153562560 | T | C | 41 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0001t0001g0223 others(38): Show |
41 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.660+4192T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562560 | |||||||
chr4:153562561 | G | A | 2 | a0001c0021t0001g0014 a0004c0018t0001g0029 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.660+4193G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562561 | |||||||
chr4:153562611 | G | A | 12 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(9): Show |
12 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.660+4243G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153562611 | |||||||
chr4:153563091 | C | G | 1 | a0002c0006t0001g0200 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.660+4723C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153563091 | |||||||
chr4:153563456 | C | CT | 89 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(86): Show |
89 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.660+5117dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153563456 | ||||||
chr4:153563456 | C | CTT | 16 | a0001c0001t0001g0039 a0001c0001t0001g0236 a0001c0001t0002g0063 others(13): Show |
16 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.660+5116_660+5117d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153563456 | ||||||
chr4:153563456 | C | CTTT | 6 | a0001c0002t0002g0065 a0001c0024t0001g0015 a0001c0041t0001g0220 others(3): Show |
6 | HG01123.hp2 HG01258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+5115_660+5117d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153563456 | ||||||
chr4:153563456 | CTTTTT | C | 15 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0005t0001g0022 others(12): Show |
15 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.660+5113_660+5117d others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153563456 | ||||||
chr4:153563456 | CTTTTTT | C | 5 | a0001c0005t0001g0038 a0001c0005t0001g0232 a0001c0008t0001g0204 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.660+5112_660+5117d others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153563456 | ||||||
chr4:153563456 | CTTTTTTT | C | 11 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(8): Show |
11 | HG02559.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.660+5111_660+5117d others(9): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153563456 | ||||||
chr4:153563456 | CTTTTTTT others(4): Show |
C | 1 | a0001c0005t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.660+5107_660+5117d others(13): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153563456 | ||||||
chr4:153563464 | T | C | 2 | a0002c0007t0001g0228 a0002c0007t0001g0231 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.660+5096T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153563464 | |||||||
chr4:153563592 | C | T | 1 | a0001c0005t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.660+5224C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153563592 | |||||||
chr4:153563805 | G | A | 1 | a0001c0021t0001g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.660+5437G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153563805 | |||||||
chr4:153564017 | G | A | 10 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
10 | HG02622.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.660+5649G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564017 | |||||||
chr4:153564176 | C | A | 2 | a0001c0002t0001g0045 a0002c0015t0001g0046 |
2 | NA18953.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.660+5808C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564176 | |||||||
chr4:153564237 | T | C | 32 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0001t0001g0223 others(29): Show |
32 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+5869T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564237 | |||||||
chr4:153564270 | C | CAA | 32 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0001t0001g0223 others(29): Show |
32 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+5902_660+5903i others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564270 | |||||||
chr4:153564282 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.660+5914C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564282 | |||||||
chr4:153564287 | C | CA | 60 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(57): Show |
60 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.660+5946dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564287 | C | CAA | 6 | a0001c0001t0001g0041 a0001c0001t0001g0227 a0001c0002t0001g0007 others(3): Show |
6 | HG02258.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+5945_660+5946d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564287 | C | CAAAAA | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
10 | HG02486.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.660+5942_660+5946d others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564287 | C | CAAAAAAA | 8 | a0001c0001t0001g0219 a0001c0005t0001g0022 a0001c0024t0001g0010 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+5940_660+5946d others(9): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564287 | C | CAAAAAAA others(5): Show |
1 | a0004c0018t0001g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.660+5935_660+5946d others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564287 | C | CAAAAAAA others(8): Show |
1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.660+5932_660+5946d others(17): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564287 | C | CAAAAAAA others(49): Show |
1 | a0001c0021t0001g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.660+5946_660+5947i others(58): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564287 | CA | C | 8 | a0001c0002t0001g0024 a0001c0002t0002g0065 a0001c0002t0002g0081 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.660+5946delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564287 | CAAAAAAA others(7): Show |
C | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.660+5933_660+5946d others(16): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153564287 | ||||||
chr4:153564314 | A | G | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.660+5946A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564314 | |||||||
chr4:153564336 | C | A | 2 | a0001c0021t0001g0014 a0004c0018t0001g0029 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.660+5968C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564336 | |||||||
chr4:153564354 | A | T | 1 | a0001c0004t0001g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.660+5986A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564354 | |||||||
chr4:153564604 | G | C | 4 | a0001c0002t0001g0017 a0001c0003t0001g0178 a0001c0003t0001g0206 others(1): Show |
4 | HG02300.hp2 HG02559.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+6236G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564604 | |||||||
chr4:153564664 | T | C | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.660+6296T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564664 | |||||||
chr4:153564777 | G | A | 8 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
8 | HG02622.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.660+6409G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153564777 | |||||||
chr4:153565047 | A | T | 1 | a0002c0010t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.660+6679A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153565047 | |||||||
chr4:153565059 | G | A | 32 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0001t0001g0223 others(29): Show |
32 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+6691G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153565059 | |||||||
chr4:153565276 | A | G | 2 | a0001c0003t0001g0182 a0001c0003t0001g0183 |
2 | HG00140.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.660+6908A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153565276 | |||||||
chr4:153565387 | G | T | 9 | a0001c0004t0001g0115 a0001c0004t0001g0127 a0001c0004t0001g0134 others(6): Show |
9 | HG01346.hp2 HG01361.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+7019G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153565387 | |||||||
chr4:153565400 | C | T | 32 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0001t0001g0223 others(29): Show |
32 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+7032C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153565400 | |||||||
chr4:153565417 | T | G | 2 | a0001c0002t0001g0054 a0001c0047t0001g0159 |
2 | HG02071.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.660+7049T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153565417 | |||||||
chr4:153565445 | T | G | 3 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0081 |
3 | HG01891.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.660+7077T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153565445 | |||||||
chr4:153565724 | AATTTG | A | 32 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0001t0001g0223 others(29): Show |
32 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+7359_660+7363d others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153565724 | ||||||
chr4:153566137 | CT | C | 9 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
9 | HG02615.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+7784delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566137 | ||||||
chr4:153566193 | T | C | 4 | a0001c0005t0001g0038 a0001c0005t0001g0232 a0001c0008t0001g0204 others(1): Show |
4 | HG02572.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+7825T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566193 | |||||||
chr4:153566237 | G | A | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.660+7869G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566237 | |||||||
chr4:153566274 | C | T | 1 | a0002c0039t0001g0053 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.660+7906C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566274 | |||||||
chr4:153566314 | T | G | 1 | a0001c0001t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.660+7946T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566314 | |||||||
chr4:153566371 | G | A | 4 | a0001c0021t0001g0014 a0002c0007t0001g0229 a0004c0018t0001g0029 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+8003G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566371 | |||||||
chr4:153566377 | C | T | 8 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
8 | HG02622.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.660+8009C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566377 | |||||||
chr4:153566415 | A | G | 1 | a0001c0009t0001g0190 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.660+8047A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566415 | |||||||
chr4:153566424 | T | C | 32 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0001t0001g0223 others(29): Show |
32 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+8056T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566424 | |||||||
chr4:153566431 | G | A | 4 | a0001c0021t0001g0014 a0002c0007t0001g0229 a0004c0018t0001g0029 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+8063G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566431 | |||||||
chr4:153566480 | G | A | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.660+8112G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566480 | |||||||
chr4:153566518 | A | AGT | 83 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0025 others(80): Show |
83 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.660+8183_660+8184d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566518 | ||||||
chr4:153566518 | A | AGTGT | 15 | a0001c0001t0001g0013 a0001c0002t0001g0002 a0001c0002t0001g0047 others(12): Show |
15 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.660+8181_660+8184d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566518 | ||||||
chr4:153566518 | A | AGTGTGT | 4 | a0001c0004t0001g0214 a0001c0013t0001g0090 a0002c0010t0001g0073 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+8179_660+8184d others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566518 | ||||||
chr4:153566518 | AGT | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0086 others(15): Show |
18 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.660+8183_660+8184d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566518 | ||||||
chr4:153566518 | AGTGT | A | 12 | a0001c0001t0001g0097 a0001c0005t0001g0111 a0001c0008t0001g0194 others(9): Show |
12 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.660+8181_660+8184d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566518 | ||||||
chr4:153566518 | AGTGTGT | A | 7 | a0001c0001t0001g0219 a0001c0002t0001g0009 a0001c0002t0001g0024 others(4): Show |
7 | HG01891.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+8179_660+8184d others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566518 | ||||||
chr4:153566518 | AGTGTGTG others(3): Show |
A | 14 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(11): Show |
14 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.660+8175_660+8184d others(12): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566518 | ||||||
chr4:153566518 | AGTGTGTG others(5): Show |
A | 5 | a0001c0008t0001g0204 a0001c0021t0001g0014 a0002c0007t0001g0229 others(2): Show |
5 | HG02145.hp2 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.660+8173_660+8184d others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153566518 | ||||||
chr4:153566637 | A | G | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.660+8269A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566637 | |||||||
chr4:153566659 | G | A | 7 | a0001c0004t0001g0193 a0001c0004t0001g0212 a0001c0030t0001g0093 others(4): Show |
7 | HG00609.hp1 HG02135.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+8291G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566659 | |||||||
chr4:153566709 | A | G | 2 | a0001c0001t0001g0089 a0001c0005t0001g0221 |
2 | HG02896.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.660+8341A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566709 | |||||||
chr4:153566745 | A | G | 25 | a0001c0001t0001g0097 a0001c0001t0001g0219 a0001c0005t0001g0022 others(22): Show |
25 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.660+8377A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566745 | |||||||
chr4:153566896 | G | A | 3 | a0001c0004t0001g0135 a0001c0004t0001g0147 a0001c0004t0001g0148 |
3 | NA18955.hp2 NA18989.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.660+8528G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566896 | |||||||
chr4:153566940 | G | A | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.660+8572G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566940 | |||||||
chr4:153566992 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.660+8624C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153566992 | |||||||
chr4:153567114 | G | A | 1 | a0001c0002t0001g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.660+8746G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567114 | |||||||
chr4:153567128 | G | A | 7 | a0001c0001t0001g0097 a0001c0034t0001g0020 a0002c0006t0001g0202 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+8760G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567128 | |||||||
chr4:153567196 | A | G | 1 | a0001c0002t0001g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.660+8828A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567196 | |||||||
chr4:153567234 | T | C | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+8866T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567234 | |||||||
chr4:153567285 | T | A | 2 | a0001c0004t0001g0214 a0001c0013t0001g0090 |
2 | NA18950.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.660+8917T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567285 | |||||||
chr4:153567516 | C | G | 1 | a0002c0007t0001g0228 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.660+9148C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567516 | |||||||
chr4:153567528 | ATTT | A | 7 | a0001c0001t0001g0219 a0001c0005t0001g0022 a0001c0024t0001g0010 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+9168_660+9170d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153567528 | ||||||
chr4:153567547 | C | CT | 7 | a0001c0001t0001g0039 a0001c0001t0001g0219 a0001c0001t0002g0063 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+9193dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153567547 | ||||||
chr4:153567608 | G | A | 2 | a0001c0013t0001g0052 a0001c0014t0001g0211 |
2 | NA19060.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.660+9240G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567608 | |||||||
chr4:153567759 | T | C | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.660+9391T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567759 | |||||||
chr4:153567808 | G | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0217 a0001c0059t0001g0033 |
3 | HG02486.hp2 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.660+9440G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153567808 | |||||||
chr4:153568188 | A | G | 46 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0219 others(43): Show |
46 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.660+9820A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153568188 | |||||||
chr4:153568330 | C | T | 5 | a0001c0001t0001g0237 a0001c0005t0001g0038 a0001c0005t0001g0232 others(2): Show |
5 | HG02572.hp2 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.660+9962C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153568330 | |||||||
chr4:153568542 | T | C | 21 | a0001c0001t0001g0039 a0001c0001t0001g0237 a0001c0001t0002g0063 others(18): Show |
21 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.660+10174T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153568542 | |||||||
chr4:153568601 | C | CCTAGCAT others(5): Show |
46 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0219 others(43): Show |
46 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.660+10235_660+1023 others(16): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153568601 | ||||||
chr4:153568615 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.660+10247A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153568615 | |||||||
chr4:153568844 | G | A | 1 | a0002c0016t0001g0215 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.660+10476G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153568844 | |||||||
chr4:153569074 | A | T | 2 | a0001c0005t0001g0221 a0011c0035t0001g0035 |
2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.660+10706A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569074 | |||||||
chr4:153569176 | C | A | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.660+10808C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569176 | |||||||
chr4:153569185 | G | A | 2 | a0001c0021t0001g0014 a0004c0018t0001g0029 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.660+10817G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569185 | |||||||
chr4:153569232 | T | C | 2 | a0001c0005t0001g0221 a0011c0035t0001g0035 |
2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.660+10864T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569232 | |||||||
chr4:153569311 | T | C | 1 | a0001c0005t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.660+10943T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569311 | |||||||
chr4:153569333 | C | G | 6 | a0001c0001t0001g0097 a0002c0006t0001g0202 a0002c0006t0001g0203 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+10965C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569333 | |||||||
chr4:153569411 | C | G | 2 | a0001c0005t0001g0221 a0011c0035t0001g0035 |
2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.660+11043C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569411 | |||||||
chr4:153569544 | A | G | 39 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0219 others(36): Show |
39 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.660+11176A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569544 | |||||||
chr4:153569643 | A | G | 1 | a0001c0002t0001g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.661-11183A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569643 | |||||||
chr4:153569681 | C | A | 1 | a0001c0008t0001g0136 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.661-11145C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569681 | |||||||
chr4:153569728 | C | T | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.661-11098C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569728 | |||||||
chr4:153569749 | T | C | 3 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0081 |
3 | HG01891.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.661-11077T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569749 | |||||||
chr4:153569852 | C | T | 6 | a0001c0005t0001g0022 a0001c0024t0001g0010 a0002c0010t0001g0021 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-10974C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569852 | |||||||
chr4:153569881 | T | G | 3 | a0001c0037t0001g0230 a0002c0007t0001g0228 a0002c0007t0001g0231 |
3 | HG02622.hp2 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.661-10945T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153569881 | |||||||
chr4:153570002 | T | TTTTTA | 7 | a0001c0005t0001g0022 a0001c0024t0001g0010 a0002c0007t0001g0229 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.661-10804_661-1080 others(9): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153570002 | ||||||
chr4:153570034 | A | G | 1 | a0001c0005t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.661-10792A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570034 | |||||||
chr4:153570213 | T | C | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.661-10613T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570213 | |||||||
chr4:153570226 | A | G | 39 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0237 others(36): Show |
39 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.661-10600A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570226 | |||||||
chr4:153570245 | C | T | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.661-10581C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570245 | |||||||
chr4:153570302 | T | G | 2 | a0001c0005t0001g0221 a0011c0035t0001g0035 |
2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.661-10524T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570302 | |||||||
chr4:153570562 | G | C | 41 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0237 others(38): Show |
41 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.661-10264G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570562 | |||||||
chr4:153570885 | T | A | 10 | a0001c0001t0001g0237 a0001c0005t0001g0038 a0001c0005t0001g0232 others(7): Show |
10 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-9941T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570885 | |||||||
chr4:153570903 | T | G | 46 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0223 others(43): Show |
46 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.661-9923T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570903 | |||||||
chr4:153570988 | G | T | 8 | a0001c0001t0002g0082 a0001c0005t0001g0022 a0001c0024t0001g0010 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.661-9838G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153570988 | |||||||
chr4:153571014 | A | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0237 others(37): Show |
40 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.661-9812A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153571014 | |||||||
chr4:153571421 | T | C | 46 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0223 others(43): Show |
46 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.661-9405T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153571421 | |||||||
chr4:153571457 | C | T | 1 | a0001c0005t0001g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.661-9369C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153571457 | |||||||
chr4:153571627 | T | C | 46 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0223 others(43): Show |
46 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.661-9199T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153571627 | |||||||
chr4:153571646 | G | A | 1 | a0004c0018t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.661-9180G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153571646 | |||||||
chr4:153571972 | A | G | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-8854A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153571972 | |||||||
chr4:153571994 | C | T | 2 | a0002c0006t0001g0185 a0009c0053t0001g0179 |
2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.661-8832C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153571994 | |||||||
chr4:153572121 | A | G | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-8705A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572121 | |||||||
chr4:153572306 | AG | A | 7 | a0001c0001t0002g0082 a0001c0005t0001g0022 a0001c0024t0001g0010 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.661-8519delG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572306 | |||||||
chr4:153572368 | T | A | 1 | a0001c0008t0001g0136 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.661-8458T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572368 | |||||||
chr4:153572487 | C | T | 3 | a0001c0005t0001g0109 a0001c0008t0001g0184 a0001c0008t0001g0199 |
3 | HG01071.hp1 HG01109.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.661-8339C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572487 | |||||||
chr4:153572667 | G | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-8159G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572667 | |||||||
chr4:153572678 | C | G | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-8148C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572678 | |||||||
chr4:153572751 | A | T | 3 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0081 |
3 | HG01891.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.661-8075A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572751 | |||||||
chr4:153572797 | T | G | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-8029T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572797 | |||||||
chr4:153572881 | C | T | 1 | a0001c0005t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.661-7945C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572881 | |||||||
chr4:153572885 | G | A | 8 | a0001c0001t0002g0082 a0001c0005t0001g0022 a0001c0024t0001g0010 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.661-7941G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572885 | |||||||
chr4:153572901 | T | C | 3 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0081 |
3 | HG01891.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.661-7925T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153572901 | |||||||
chr4:153573260 | C | G | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.661-7566C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153573260 | |||||||
chr4:153573262 | C | T | 5 | a0001c0021t0001g0014 a0001c0037t0001g0230 a0002c0007t0001g0228 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-7564C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153573262 | |||||||
chr4:153573362 | A | G | 1 | a0001c0013t0001g0049 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.661-7464A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153573362 | |||||||
chr4:153573488 | A | G | 29 | a0001c0001t0001g0039 a0001c0001t0001g0237 a0001c0001t0002g0063 others(26): Show |
29 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.661-7338A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153573488 | |||||||
chr4:153573736 | C | A | 3 | a0001c0002t0001g0092 a0001c0009t0001g0158 a0001c0026t0001g0077 |
3 | HG00597.hp2 HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.661-7090C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153573736 | |||||||
chr4:153573816 | T | C | 1 | a0001c0003t0001g0201 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.661-7010T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153573816 | |||||||
chr4:153573934 | A | G | 4 | a0001c0011t0001g0105 a0001c0011t0001g0112 a0001c0022t0001g0114 others(1): Show |
4 | HG01070.hp1 HG01993.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-6892A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153573934 | |||||||
chr4:153574121 | A | AG | 37 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0223 others(34): Show |
37 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.661-6704dupG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153574121 | ||||||
chr4:153574314 | AGTG | A | 67 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0097 others(64): Show |
67 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.661-6498_661-6496d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153574314 | ||||||
chr4:153574381 | A | G | 5 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0065 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-6445A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574381 | |||||||
chr4:153574389 | A | G | 2 | a0002c0006t0001g0202 a0002c0006t0001g0203 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.661-6437A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574389 | |||||||
chr4:153574421 | A | G | 2 | a0004c0027t0001g0248 a0004c0036t0001g0234 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.661-6405A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574421 | |||||||
chr4:153574456 | G | A | 19 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0002g0063 others(16): Show |
19 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.661-6370G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574456 | |||||||
chr4:153574561 | T | C | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.661-6265T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574561 | |||||||
chr4:153574655 | A | G | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-6171A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574655 | |||||||
chr4:153574696 | C | A | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-6130C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574696 | |||||||
chr4:153574723 | G | A | 1 | a0002c0006t0001g0132 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.661-6103G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574723 | |||||||
chr4:153574819 | C | T | 2 | a0001c0005t0001g0111 a0014c0042t0001g0001 |
2 | HG01081.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.661-6007C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574819 | |||||||
chr4:153574856 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0244 a0001c0001t0002g0082 others(4): Show |
7 | HG01891.hp1 HG02717.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.661-5970G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574856 | |||||||
chr4:153574875 | A | G | 10 | a0001c0021t0001g0014 a0001c0037t0001g0230 a0002c0006t0001g0202 others(7): Show |
10 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.661-5951A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574875 | |||||||
chr4:153574887 | C | T | 4 | a0001c0002t0001g0017 a0001c0003t0001g0167 a0001c0003t0001g0178 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-5939C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153574887 | |||||||
chr4:153575173 | C | A | 2 | a0001c0001t0001g0042 a0001c0009t0001g0170 |
2 | NA18986.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.661-5653C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153575173 | |||||||
chr4:153575514 | C | T | 1 | a0002c0045t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.661-5312C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153575514 | |||||||
chr4:153575812 | G | T | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-5014G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153575812 | |||||||
chr4:153575849 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.661-4977G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153575849 | |||||||
chr4:153575971 | T | C | 1 | a0002c0055t0001g0207 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.661-4855T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153575971 | |||||||
chr4:153576048 | C | T | 1 | a0001c0004t0001g0140 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.661-4778C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576048 | |||||||
chr4:153576085 | G | A | 1 | a0002c0029t0001g0067 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.661-4741G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576085 | |||||||
chr4:153576211 | C | T | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-4615C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576211 | |||||||
chr4:153576252 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0002g0063 a0001c0002t0001g0005 others(4): Show |
7 | HG01099.hp1 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.661-4574G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576252 | |||||||
chr4:153576507 | G | C | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-4319G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576507 | |||||||
chr4:153576537 | A | T | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-4289A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576537 | |||||||
chr4:153576552 | G | T | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-4274G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576552 | |||||||
chr4:153576675 | T | TA | 5 | a0001c0004t0001g0214 a0001c0009t0001g0104 a0001c0013t0001g0052 others(2): Show |
5 | NA18943.hp1 NA18943.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-4135dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153576675 | ||||||
chr4:153576675 | TA | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0098 others(35): Show |
38 | HG00597.hp1 HG00597.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.661-4135delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153576675 | ||||||
chr4:153576675 | TAA | T | 6 | a0001c0003t0001g0181 a0002c0006t0001g0202 a0002c0006t0001g0203 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-4136_661-4135d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153576675 | ||||||
chr4:153576710 | A | C | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-4116A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576710 | |||||||
chr4:153576779 | T | C | 50 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(47): Show |
50 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.661-4047T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576779 | |||||||
chr4:153576791 | C | A | 1 | a0001c0008t0001g0187 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.661-4035C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576791 | |||||||
chr4:153576871 | C | G | 4 | a0001c0003t0001g0181 a0005c0017t0001g0026 a0005c0017t0001g0027 others(1): Show |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-3955C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576871 | |||||||
chr4:153576954 | C | T | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-3872C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576954 | |||||||
chr4:153576962 | G | T | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-3864G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576962 | |||||||
chr4:153576988 | G | A | 50 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(47): Show |
50 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.661-3838G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153576988 | |||||||
chr4:153577056 | G | A | 4 | a0001c0003t0001g0181 a0005c0017t0001g0026 a0005c0017t0001g0027 others(1): Show |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-3770G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577056 | |||||||
chr4:153577084 | T | C | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-3742T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577084 | |||||||
chr4:153577147 | C | T | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-3679C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577147 | |||||||
chr4:153577363 | A | C | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.661-3463A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577363 | |||||||
chr4:153577379 | G | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.661-3447G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577379 | |||||||
chr4:153577404 | A | G | 50 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(47): Show |
50 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.661-3422A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577404 | |||||||
chr4:153577570 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0227 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-3256A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577570 | |||||||
chr4:153577725 | G | A | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-3101G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577725 | |||||||
chr4:153577780 | G | T | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.661-3046G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577780 | |||||||
chr4:153577949 | G | A | 18 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0098 others(15): Show |
18 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.661-2877G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153577949 | |||||||
chr4:153578168 | C | T | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.661-2658C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578168 | |||||||
chr4:153578229 | G | A | 2 | a0001c0008t0001g0194 a0001c0034t0001g0020 |
2 | HG03710.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.661-2597G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578229 | |||||||
chr4:153578270 | C | A | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-2556C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578270 | |||||||
chr4:153578418 | T | C | 51 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(48): Show |
51 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(48): Show |
intron_variant | MODIFIER | c.661-2408T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578418 | |||||||
chr4:153578465 | C | T | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-2361C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578465 | |||||||
chr4:153578522 | G | GT | 32 | a0001c0001t0001g0025 a0001c0002t0001g0054 a0001c0002t0002g0065 others(29): Show |
32 | HG00408.hp2 HG00558.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.661-2286dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153578522 | ||||||
chr4:153578559 | C | T | 6 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0081 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2267C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578559 | |||||||
chr4:153578583 | C | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0098 others(16): Show |
19 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.661-2243C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578583 | |||||||
chr4:153578687 | ATTTTTTG others(129): Show |
A | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.661-2102_661-1967d others(2): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153578687 | ||||||
chr4:153578714 | G | C | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-2112G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578714 | |||||||
chr4:153578850 | GTT | G | 6 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0081 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-1974_661-1973d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153578850 | ||||||
chr4:153578871 | T | G | 2 | a0001c0005t0001g0111 a0014c0042t0001g0001 |
2 | HG01081.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.661-1955T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578871 | |||||||
chr4:153578919 | A | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0098 others(23): Show |
26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.661-1907A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578919 | |||||||
chr4:153578949 | C | T | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.661-1877C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578949 | |||||||
chr4:153578988 | T | A | 1 | a0001c0002t0002g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661-1838T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578988 | |||||||
chr4:153578992 | A | G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-1834A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153578992 | |||||||
chr4:153579297 | C | T | 1 | a0003c0023t0001g0083 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.661-1529C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579297 | |||||||
chr4:153579437 | T | C | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-1389T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579437 | |||||||
chr4:153579541 | G | A | 42 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(39): Show |
42 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.661-1285G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579541 | |||||||
chr4:153579561 | T | C | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-1265T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579561 | |||||||
chr4:153579616 | C | T | 1 | a0001c0014t0001g0138 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.661-1210C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579616 | |||||||
chr4:153579755 | G | A | 10 | a0001c0004t0001g0115 a0001c0004t0001g0127 a0001c0004t0001g0134 others(7): Show |
10 | HG01346.hp2 HG01361.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.661-1071G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579755 | |||||||
chr4:153579822 | A | G | 1 | a0001c0004t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.661-1004A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579822 | |||||||
chr4:153579828 | A | AAATGTAT others(3027): Show |
1 | a0002c0010t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.661-985_661-984ins others(3034): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153579828 | ||||||
chr4:153579867 | A | T | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.661-959A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579867 | |||||||
chr4:153579976 | C | T | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-850C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153579976 | |||||||
chr4:153580028 | C | G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-798C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153580028 | |||||||
chr4:153580029 | T | G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661-797T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153580029 | |||||||
chr4:153580099 | A | G | 2 | a0001c0004t0001g0189 a0001c0004t0001g0197 |
2 | NA18944.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.661-727A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153580099 | |||||||
chr4:153580115 | CTT | C | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-707_661-706del others(2): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr4 | 153580115 | ||||||
chr4:153580358 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(42): Show |
45 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.661-468G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153580358 | |||||||
chr4:153580580 | C | T | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-246C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153580580 | |||||||
chr4:153580596 | T | C | 1 | a0001c0002t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.661-230T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153580596 | |||||||
chr4:153580665 | G | A | 50 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(47): Show |
50 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.661-161G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153580665 | |||||||
chr4:153580706 | T | A | 1 | a0001c0012t0001g0169 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.661-120T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 7/34 | chr4 | 153580706 | |||||||
chr4:153580916 | G | A | 50 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(47): Show |
50 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.738+13G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153580916 | |||||||
chr4:153580952 | T | C | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.738+49T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153580952 | |||||||
chr4:153580991 | T | G | 2 | a0001c0003t0001g0163 a0001c0012t0001g0162 |
2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.738+88T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153580991 | |||||||
chr4:153581023 | G | A | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.738+120G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153581023 | |||||||
chr4:153581069 | C | T | 2 | a0001c0004t0001g0171 a0001c0012t0001g0149 |
2 | HG00408.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.738+166C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153581069 | |||||||
chr4:153581130 | C | T | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.738+227C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153581130 | |||||||
chr4:153581185 | C | T | 3 | a0001c0005t0001g0106 a0001c0005t0001g0232 a0001c0028t0001g0108 |
3 | HG01884.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.739-222C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153581185 | |||||||
chr4:153581268 | TAAAATAA others(3): Show |
T | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.739-137_739-128del others(10): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr4 | 153581268 | ||||||
chr4:153581340 | C | G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.739-67C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153581340 | |||||||
chr4:153581403 | A | G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.739-4A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 8/34 | chr4 | 153581403 | |||||||
chr4:153581589 | A | C | 7 | a0001c0003t0001g0182 a0001c0003t0001g0183 a0001c0008t0001g0176 others(4): Show |
7 | HG00140.hp2 HG00735.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.892+29A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153581589 | |||||||
chr4:153581689 | G | A | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.892+129G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153581689 | |||||||
chr4:153581787 | AT | A | 47 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(44): Show |
47 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.892+232delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153581787 | ||||||
chr4:153581796 | C | A | 1 | a0001c0009t0001g0192 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.892+236C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153581796 | |||||||
chr4:153581890 | T | C | 2 | a0001c0004t0001g0125 a0001c0014t0001g0138 |
2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.892+330T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153581890 | |||||||
chr4:153581957 | G | A | 1 | a0002c0016t0001g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.892+397G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153581957 | |||||||
chr4:153582036 | C | G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.892+476C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582036 | |||||||
chr4:153582126 | A | G | 1 | a0008c0052t0001g0120 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.892+566A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582126 | |||||||
chr4:153582178 | T | A | 50 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(47): Show |
50 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.892+618T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582178 | |||||||
chr4:153582303 | G | T | 5 | a0001c0001t0001g0089 a0001c0003t0001g0119 a0001c0009t0001g0145 others(2): Show |
5 | HG01496.hp2 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.892+743G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582303 | |||||||
chr4:153582313 | C | T | 39 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(36): Show |
39 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.892+753C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582313 | |||||||
chr4:153582419 | CGTTTTTT others(6): Show |
C | 2 | a0002c0006t0001g0203 a0002c0007t0001g0070 |
2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.893-760_893-748del others(13): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582419 | ||||||
chr4:153582420 | GTTTTTTT others(7): Show |
G | 3 | a0002c0006t0001g0202 a0002c0007t0001g0023 a0002c0007t0001g0096 |
3 | HG01884.hp1 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.893-760_893-747del others(14): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582420 | ||||||
chr4:153582420 | GTTTTTTT others(11): Show |
G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.893-760_893-743del others(18): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582420 | ||||||
chr4:153582421 | TTTTTTTT others(5): Show |
T | 4 | a0001c0002t0001g0009 a0001c0034t0001g0020 a0001c0037t0001g0230 others(1): Show |
4 | HG02976.hp2 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.893-760_893-749del others(12): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582421 | ||||||
chr4:153582422 | TTTTTTTT others(4): Show |
T | 6 | a0001c0001t0001g0039 a0001c0001t0002g0063 a0001c0002t0001g0024 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-760_893-750del others(11): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582422 | ||||||
chr4:153582423 | TTTTTTTG others(3): Show |
T | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0226 others(4): Show |
7 | HG02257.hp1 HG02615.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-760_893-751del others(10): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582423 | ||||||
chr4:153582424 | TTTTTTGT others(2): Show |
T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0098 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.893-760_893-752del others(9): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582424 | ||||||
chr4:153582425 | TTTTTGTT others(1): Show |
T | 7 | a0001c0005t0001g0247 a0001c0024t0001g0010 a0002c0007t0001g0228 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.893-760_893-753del others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582425 | ||||||
chr4:153582430 | G | T | 3 | a0001c0002t0002g0065 a0001c0024t0001g0015 a0001c0041t0001g0220 |
3 | HG02630.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.893-760G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582430 | |||||||
chr4:153582433 | G | GT | 97 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0042 others(94): Show |
97 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.893-731dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582433 | ||||||
chr4:153582433 | G | GTT | 15 | a0001c0001t0001g0025 a0001c0001t0001g0227 a0001c0003t0001g0163 others(12): Show |
15 | HG00735.hp2 HG01346.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.893-732_893-731dup others(2): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr4 | 153582433 | ||||||
chr4:153582433 | G | T | 9 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0002t0002g0065 others(6): Show |
9 | HG01109.hp2 HG01192.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.893-757G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582433 | |||||||
chr4:153582517 | A | C | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.893-673A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582517 | |||||||
chr4:153582664 | C | T | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.893-526C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582664 | |||||||
chr4:153582768 | C | T | 42 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(39): Show |
42 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.893-422C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582768 | |||||||
chr4:153582890 | C | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0098 others(15): Show |
18 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.893-300C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582890 | |||||||
chr4:153582901 | G | A | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.893-289G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153582901 | |||||||
chr4:153583004 | T | C | 1 | a0002c0006t0001g0200 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.893-186T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153583004 | |||||||
chr4:153583028 | C | G | 4 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0002g0081 others(1): Show |
4 | HG01891.hp1 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-162C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 9/34 | chr4 | 153583028 | |||||||
chr4:153583363 | CTTTAA | C | 39 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(36): Show |
39 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.951+121_951+125del others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 10/34 | INFO_REALIGN_3_PRIME | chr4 | 153583363 | ||||||
chr4:153583385 | C | G | 2 | a0002c0007t0001g0228 a0002c0007t0001g0231 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.951+137C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 10/34 | chr4 | 153583385 | |||||||
chr4:153583405 | T | C | 2 | a0001c0004t0001g0171 a0001c0012t0001g0149 |
2 | HG00408.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.951+157T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 10/34 | chr4 | 153583405 | |||||||
chr4:153583739 | T | C | 1 | a0002c0025t0001g0166 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1060+67T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153583739 | |||||||
chr4:153583813 | A | G | 6 | a0001c0001t0001g0039 a0001c0001t0002g0063 a0001c0005t0001g0111 others(3): Show |
6 | HG01081.hp2 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060+141A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153583813 | |||||||
chr4:153583899 | A | G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1060+227A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153583899 | |||||||
chr4:153583961 | G | T | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060+289G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153583961 | |||||||
chr4:153583987 | ATCTC | A | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1060+317_1060+320d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr4 | 153583987 | ||||||
chr4:153583993 | A | G | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060+321A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153583993 | |||||||
chr4:153584084 | C | T | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1060+412C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584084 | |||||||
chr4:153584175 | G | C | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1060+503G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584175 | |||||||
chr4:153584283 | C | T | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1061-552C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584283 | |||||||
chr4:153584338 | G | A | 8 | a0001c0005t0001g0022 a0001c0024t0001g0010 a0002c0007t0001g0228 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1061-497G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584338 | |||||||
chr4:153584422 | G | T | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1061-413G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584422 | |||||||
chr4:153584435 | A | G | 1 | a0001c0011t0001g0079 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1061-400A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584435 | |||||||
chr4:153584436 | T | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0098 others(15): Show |
18 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1061-399T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584436 | |||||||
chr4:153584515 | C | G | 2 | a0001c0024t0001g0015 a0001c0041t0001g0220 |
2 | HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1061-320C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584515 | |||||||
chr4:153584763 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1061-72A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584763 | |||||||
chr4:153584765 | A | G | 42 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(39): Show |
42 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1061-70A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584765 | |||||||
chr4:153584801 | T | G | 2 | a0001c0004t0001g0193 a0001c0004t0001g0212 |
2 | HG02135.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1061-34T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 11/34 | chr4 | 153584801 | |||||||
chr4:153585040 | A | G | 51 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(48): Show |
51 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(48): Show |
intron_variant | MODIFIER | c.1157+109A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 12/34 | chr4 | 153585040 | |||||||
chr4:153585244 | T | C | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1158-214T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 12/34 | chr4 | 153585244 | |||||||
chr4:153585317 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1158-141C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 12/34 | chr4 | 153585317 | |||||||
chr4:153585709 | C | A | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1311+98C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 13/34 | chr4 | 153585709 | |||||||
chr4:153586165 | T | G | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-44T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 13/34 | chr4 | 153586165 | |||||||
chr4:153586441 | C | G | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1482+62C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153586441 | |||||||
chr4:153586469 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1482+90G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153586469 | |||||||
chr4:153586480 | G | A | 1 | a0001c0005t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1482+101G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153586480 | |||||||
chr4:153586520 | G | A | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1482+141G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153586520 | |||||||
chr4:153586600 | T | G | 16 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0098 others(13): Show |
16 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1482+221T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153586600 | |||||||
chr4:153586727 | A | G | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1482+348A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153586727 | |||||||
chr4:153586937 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1482+558G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153586937 | |||||||
chr4:153587047 | G | A | 4 | a0001c0001t0001g0237 a0001c0002t0001g0005 a0001c0002t0001g0217 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+668G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153587047 | |||||||
chr4:153587055 | T | G | 2 | a0001c0024t0001g0015 a0001c0041t0001g0220 |
2 | HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1482+676T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153587055 | |||||||
chr4:153587216 | G | A | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1483-526G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153587216 | |||||||
chr4:153587287 | T | C | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1483-455T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153587287 | |||||||
chr4:153587329 | TA | T | 42 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0095 others(39): Show |
42 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1483-404delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr4 | 153587329 | ||||||
chr4:153587446 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1483-296C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153587446 | |||||||
chr4:153587528 | A | G | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1483-214A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153587528 | |||||||
chr4:153587579 | A | G | 1 | a0012c0032t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1483-163A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 14/34 | chr4 | 153587579 | |||||||
chr4:153587877 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1552+66A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | chr4 | 153587877 | |||||||
chr4:153588041 | G | GT | 8 | a0001c0001t0001g0012 a0001c0002t0001g0047 a0001c0003t0001g0122 others(5): Show |
8 | HG01891.hp2 HG02135.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1552+247dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr4 | 153588041 | ||||||
chr4:153588041 | GT | G | 54 | a0001c0001t0001g0039 a0001c0001t0001g0223 a0001c0001t0001g0224 others(51): Show |
54 | HG01081.hp2 HG01243.hp2 HG01361.hp2 others(51): Show |
intron_variant | MODIFIER | c.1552+247delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr4 | 153588041 | ||||||
chr4:153588129 | A | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1552+318A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | chr4 | 153588129 | |||||||
chr4:153588241 | G | A | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1552+430G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | chr4 | 153588241 | |||||||
chr4:153588272 | G | GT | 6 | a0001c0003t0001g0181 a0003c0019t0001g0154 a0003c0019t0001g0198 others(3): Show |
6 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1552+472dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr4 | 153588272 | ||||||
chr4:153588273 | T | G | 1 | a0001c0012t0001g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1552+462T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | chr4 | 153588273 | |||||||
chr4:153588284 | G | GT | 8 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0001g0051 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1552+481dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr4 | 153588284 | ||||||
chr4:153588337 | G | GT | 25 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0227 others(22): Show |
25 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1553-536dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr4 | 153588337 | ||||||
chr4:153588337 | G | GTT | 28 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0095 others(25): Show |
28 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1553-537_1553-536d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr4 | 153588337 | ||||||
chr4:153588337 | G | GTTT | 6 | a0001c0001t0001g0039 a0001c0001t0002g0063 a0001c0033t0001g0099 others(3): Show |
6 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1553-538_1553-536d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr4 | 153588337 | ||||||
chr4:153588337 | GT | G | 5 | a0001c0002t0001g0113 a0001c0005t0001g0221 a0001c0011t0001g0243 others(2): Show |
5 | HG01099.hp1 HG02523.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1553-536delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr4 | 153588337 | ||||||
chr4:153588599 | T | C | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1553-291T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | chr4 | 153588599 | |||||||
chr4:153588620 | T | A | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1553-270T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 15/34 | chr4 | 153588620 | |||||||
chr4:153589092 | A | G | 10 | a0001c0004t0001g0115 a0001c0004t0001g0127 a0001c0004t0001g0134 others(7): Show |
10 | HG01346.hp2 HG01361.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1670+85A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589092 | |||||||
chr4:153589120 | G | A | 1 | a0001c0037t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1670+113G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589120 | |||||||
chr4:153589205 | C | T | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1670+198C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589205 | |||||||
chr4:153589424 | C | T | 8 | a0001c0024t0001g0010 a0002c0007t0001g0228 a0002c0007t0001g0231 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1670+417C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589424 | |||||||
chr4:153589691 | G | A | 44 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(41): Show |
44 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1670+684G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589691 | |||||||
chr4:153589751 | G | C | 6 | a0001c0003t0001g0181 a0003c0019t0001g0154 a0003c0019t0001g0198 others(3): Show |
6 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1670+744G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589751 | |||||||
chr4:153589829 | T | G | 1 | a0001c0002t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1670+822T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589829 | |||||||
chr4:153589986 | A | G | 6 | a0001c0003t0001g0181 a0003c0019t0001g0154 a0003c0019t0001g0198 others(3): Show |
6 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1670+979A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589986 | |||||||
chr4:153589994 | A | G | 1 | a0002c0025t0001g0103 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1670+987A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153589994 | |||||||
chr4:153590166 | G | C | 6 | a0001c0003t0001g0181 a0003c0019t0001g0154 a0003c0019t0001g0198 others(3): Show |
6 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-887G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153590166 | |||||||
chr4:153590386 | G | A | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1671-667G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153590386 | |||||||
chr4:153590429 | C | T | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1671-624C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153590429 | |||||||
chr4:153590525 | C | T | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0002t0002g0065 |
3 | HG02647.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1671-528C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153590525 | |||||||
chr4:153590668 | T | A | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-385T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153590668 | |||||||
chr4:153590680 | A | G | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1671-373A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153590680 | |||||||
chr4:153590832 | C | CTGT | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1671-216_1671-214d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr4 | 153590832 | ||||||
chr4:153590861 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1671-192G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 16/34 | chr4 | 153590861 | |||||||
chr4:153591285 | A | G | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1812+91A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153591285 | |||||||
chr4:153591360 | GAAAC | G | 20 | a0001c0001t0001g0098 a0001c0001t0001g0223 a0001c0001t0001g0224 others(17): Show |
20 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1812+170_1812+173d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | INFO_REALIGN_3_PRIME | chr4 | 153591360 | ||||||
chr4:153591504 | C | T | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1812+310C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153591504 | |||||||
chr4:153591561 | A | C | 8 | a0002c0007t0001g0228 a0002c0007t0001g0229 a0002c0007t0001g0231 others(5): Show |
8 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1812+367A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153591561 | |||||||
chr4:153591609 | C | T | 1 | a0001c0002t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1812+415C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153591609 | |||||||
chr4:153591765 | G | A | 1 | a0001c0014t0001g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1812+571G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153591765 | |||||||
chr4:153591788 | T | C | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1812+594T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153591788 | |||||||
chr4:153591902 | A | G | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1813-573A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153591902 | |||||||
chr4:153591995 | C | T | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1813-480C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153591995 | |||||||
chr4:153592046 | T | C | 1 | a0001c0005t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1813-429T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153592046 | |||||||
chr4:153592129 | C | T | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1813-346C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153592129 | |||||||
chr4:153592208 | AT | A | 44 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0098 others(41): Show |
44 | HG01243.hp2 HG01257.hp1 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.1813-256delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | INFO_REALIGN_3_PRIME | chr4 | 153592208 | ||||||
chr4:153592379 | A | G | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1813-96A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153592379 | |||||||
chr4:153592398 | A | G | 1 | a0002c0015t0001g0046 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1813-77A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 17/34 | chr4 | 153592398 | |||||||
chr4:153592652 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1922+68C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153592652 | |||||||
chr4:153592704 | G | C | 102 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0097 others(99): Show |
102 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1922+120G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153592704 | |||||||
chr4:153592775 | G | C | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1922+191G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153592775 | |||||||
chr4:153592907 | A | G | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1922+323A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153592907 | |||||||
chr4:153592997 | C | A | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1922+413C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153592997 | |||||||
chr4:153593071 | G | A | 1 | a0013c0058t0001g0031 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1922+487G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593071 | |||||||
chr4:153593268 | C | T | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(1): Show |
4 | HG01109.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923-531C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593268 | |||||||
chr4:153593269 | G | T | 5 | a0001c0003t0001g0182 a0001c0003t0001g0183 a0001c0008t0001g0176 others(2): Show |
5 | HG00140.hp2 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1923-530G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593269 | |||||||
chr4:153593327 | A | G | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1923-472A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593327 | |||||||
chr4:153593393 | A | C | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1923-406A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593393 | |||||||
chr4:153593428 | C | T | 1 | a0003c0054t0001g0123 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1923-371C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593428 | |||||||
chr4:153593446 | G | A | 5 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0210 others(2): Show |
5 | HG00558.hp1 NA18972.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1923-353G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593446 | |||||||
chr4:153593501 | T | G | 4 | a0001c0002t0001g0017 a0001c0003t0001g0167 a0001c0003t0001g0178 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923-298T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593501 | |||||||
chr4:153593604 | TGTGGGAA others(16): Show |
T | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 |
3 | HG02647.hp1 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1923-176_1923-154d others(25): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr4 | 153593604 | ||||||
chr4:153593648 | G | A | 7 | a0001c0003t0001g0181 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1923-151G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593648 | |||||||
chr4:153593695 | T | C | 45 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(42): Show |
45 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1923-104T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593695 | |||||||
chr4:153593766 | T | C | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1923-33T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 18/34 | chr4 | 153593766 | |||||||
chr4:153593882 | A | G | 1 | a0001c0002t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1995+11A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153593882 | |||||||
chr4:153593995 | C | T | 1 | a0001c0008t0001g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1995+124C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153593995 | |||||||
chr4:153594021 | A | G | 1 | a0001c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1995+150A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594021 | |||||||
chr4:153594022 | T | C | 2 | a0001c0005t0001g0247 a0001c0008t0001g0128 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1995+151T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594022 | |||||||
chr4:153594198 | T | G | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1995+327T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594198 | |||||||
chr4:153594235 | T | TA | 8 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0236 others(5): Show |
8 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1995+372dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr4 | 153594235 | ||||||
chr4:153594241 | A | G | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+370A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594241 | |||||||
chr4:153594243 | AT | A | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+373delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594243 | |||||||
chr4:153594352 | G | A | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+481G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594352 | |||||||
chr4:153594402 | G | C | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+531G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594402 | |||||||
chr4:153594405 | G | T | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+534G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594405 | |||||||
chr4:153594466 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 |
3 | HG02647.hp1 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1995+595G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594466 | |||||||
chr4:153594584 | C | T | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+713C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594584 | |||||||
chr4:153594604 | A | G | 7 | a0001c0003t0001g0181 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1995+733A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594604 | |||||||
chr4:153594704 | G | A | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+833G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594704 | |||||||
chr4:153594825 | C | T | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+954C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594825 | |||||||
chr4:153594908 | G | A | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+1037G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594908 | |||||||
chr4:153594969 | G | A | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+1098G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153594969 | |||||||
chr4:153595029 | G | A | 103 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0097 others(100): Show |
103 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.1995+1158G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595029 | |||||||
chr4:153595048 | G | A | 53 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(50): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1995+1177G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595048 | |||||||
chr4:153595182 | T | G | 1 | a0001c0002t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1996-1076T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595182 | |||||||
chr4:153595195 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1996-1063T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595195 | |||||||
chr4:153595347 | A | G | 1 | a0008c0052t0001g0120 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1996-911A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595347 | |||||||
chr4:153595411 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 |
3 | HG02647.hp1 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1996-847G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595411 | |||||||
chr4:153595450 | GAATCAAA others(1): Show |
G | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1996-798_1996-791d others(10): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr4 | 153595450 | ||||||
chr4:153595527 | A | C | 7 | a0001c0003t0001g0181 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1996-731A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595527 | |||||||
chr4:153595587 | G | A | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1996-671G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595587 | |||||||
chr4:153595650 | C | G | 2 | a0001c0003t0001g0182 a0001c0003t0001g0183 |
2 | HG00140.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1996-608C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595650 | |||||||
chr4:153595714 | C | CA | 9 | a0001c0001t0001g0041 a0001c0002t0001g0019 a0001c0002t0001g0100 others(6): Show |
9 | HG02148.hp2 HG03017.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.1996-529dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr4 | 153595714 | ||||||
chr4:153595714 | C | CAA | 7 | a0001c0003t0001g0181 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1996-530_1996-529d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr4 | 153595714 | ||||||
chr4:153595714 | CA | C | 17 | a0001c0001t0001g0098 a0001c0001t0001g0223 a0001c0001t0001g0224 others(14): Show |
17 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1996-529delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr4 | 153595714 | ||||||
chr4:153595724 | A | AAAAC | 54 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(51): Show |
54 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1996-531_1996-530i others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr4 | 153595724 | ||||||
chr4:153595724 | A | C | 2 | a0002c0006t0001g0202 a0002c0006t0001g0203 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1996-534A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595724 | |||||||
chr4:153595930 | G | A | 7 | a0001c0003t0001g0181 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1996-328G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153595930 | |||||||
chr4:153596016 | A | G | 1 | a0001c0005t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1996-242A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153596016 | |||||||
chr4:153596063 | A | G | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1996-195A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153596063 | |||||||
chr4:153596142 | G | T | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1996-116G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153596142 | |||||||
chr4:153596154 | G | C | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1996-104G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 19/34 | chr4 | 153596154 | |||||||
chr4:153596699 | C | T | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2123+314C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153596699 | |||||||
chr4:153596714 | T | C | 1 | a0001c0003t0001g0119 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2123+329T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153596714 | |||||||
chr4:153596877 | G | A | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2123+492G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153596877 | |||||||
chr4:153597132 | G | A | 6 | a0001c0002t0001g0060 a0001c0003t0001g0182 a0001c0003t0001g0183 others(3): Show |
6 | HG00140.hp2 HG01071.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2123+747G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597132 | |||||||
chr4:153597160 | A | G | 35 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0098 others(32): Show |
35 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.2123+775A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597160 | |||||||
chr4:153597175 | C | A | 95 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0098 others(92): Show |
95 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.2123+790C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597175 | |||||||
chr4:153597192 | G | A | 7 | a0001c0003t0001g0181 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.2123+807G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597192 | |||||||
chr4:153597273 | AT | A | 57 | a0001c0002t0002g0065 a0002c0006t0001g0118 a0002c0006t0001g0130 others(54): Show |
57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2123+899delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr4 | 153597273 | ||||||
chr4:153597428 | C | T | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2123+1043C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597428 | |||||||
chr4:153597473 | G | T | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2123+1088G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597473 | |||||||
chr4:153597839 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2124-751A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597839 | |||||||
chr4:153597850 | G | A | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2124-740G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597850 | |||||||
chr4:153597921 | A | C | 1 | a0012c0032t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2124-669A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597921 | |||||||
chr4:153597954 | T | A | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2124-636T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597954 | |||||||
chr4:153597997 | A | G | 36 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0098 others(33): Show |
36 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.2124-593A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153597997 | |||||||
chr4:153598055 | G | GTTA | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2124-532_2124-530d others(5): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr4 | 153598055 | ||||||
chr4:153598066 | G | A | 1 | a0002c0010t0001g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2124-524G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153598066 | |||||||
chr4:153598112 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0098 others(33): Show |
36 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.2124-478G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153598112 | |||||||
chr4:153598243 | GT | G | 58 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(55): Show |
58 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.2124-336delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr4 | 153598243 | ||||||
chr4:153598506 | A | G | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2124-84A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153598506 | |||||||
chr4:153598514 | G | C | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2124-76G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153598514 | |||||||
chr4:153598527 | T | C | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2124-63T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 20/34 | chr4 | 153598527 | |||||||
chr4:153598919 | C | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0098 others(33): Show |
36 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.2266+187C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153598919 | |||||||
chr4:153599052 | C | CAA | 55 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0164 others(52): Show |
55 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.2266+321_2266+322d others(4): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr4 | 153599052 | ||||||
chr4:153599055 | G | A | 1 | a0002c0006t0001g0132 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2266+323G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599055 | |||||||
chr4:153599266 | G | A | 56 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(53): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2266+534G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599266 | |||||||
chr4:153599317 | G | C | 60 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(57): Show |
60 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2266+585G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599317 | |||||||
chr4:153599409 | A | G | 78 | a0001c0001t0001g0098 a0001c0001t0001g0223 a0001c0001t0001g0224 others(75): Show |
78 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.2266+677A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599409 | |||||||
chr4:153599451 | G | A | 60 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(57): Show |
60 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2266+719G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599451 | |||||||
chr4:153599508 | T | C | 67 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(64): Show |
67 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2266+776T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599508 | |||||||
chr4:153599510 | C | T | 2 | a0002c0007t0001g0072 a0010c0038t0001g0056 |
2 | HG01192.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2266+778C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599510 | |||||||
chr4:153599541 | A | G | 11 | a0002c0007t0001g0228 a0002c0007t0001g0229 a0002c0007t0001g0231 others(8): Show |
11 | HG02109.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2266+809A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599541 | |||||||
chr4:153599628 | T | C | 60 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(57): Show |
60 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2266+896T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599628 | |||||||
chr4:153599781 | A | G | 59 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(56): Show |
59 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2266+1049A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599781 | |||||||
chr4:153599891 | C | T | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 |
3 | HG02647.hp1 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2266+1159C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599891 | |||||||
chr4:153599952 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2266+1220C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153599952 | |||||||
chr4:153600095 | T | A | 4 | a0001c0021t0001g0014 a0001c0024t0001g0015 a0001c0037t0001g0230 others(1): Show |
4 | HG02145.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2266+1363T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600095 | |||||||
chr4:153600107 | A | G | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2266+1375A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600107 | |||||||
chr4:153600157 | G | A | 57 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(54): Show |
57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2266+1425G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600157 | |||||||
chr4:153600337 | A | C | 57 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(54): Show |
57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2266+1605A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600337 | |||||||
chr4:153600340 | G | A | 1 | a0001c0005t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2266+1608G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600340 | |||||||
chr4:153600368 | GA | G | 8 | a0001c0001t0001g0039 a0003c0019t0001g0153 a0003c0019t0001g0154 others(5): Show |
8 | HG01243.hp2 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2266+1651delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr4 | 153600368 | ||||||
chr4:153600368 | GAA | G | 57 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(54): Show |
57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2266+1650_2266+165 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr4 | 153600368 | ||||||
chr4:153600387 | CAAAAAT | C | 8 | a0002c0007t0001g0228 a0002c0007t0001g0229 a0002c0007t0001g0231 others(5): Show |
8 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2266+1664_2266+166 others(10): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr4 | 153600387 | ||||||
chr4:153600422 | G | A | 66 | a0001c0001t0001g0039 a0001c0001t0002g0061 a0001c0001t0002g0062 others(63): Show |
66 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.2266+1690G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600422 | |||||||
chr4:153600444 | G | C | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 |
3 | HG02647.hp1 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2267-1708G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600444 | |||||||
chr4:153600511 | G | A | 57 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(54): Show |
57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2267-1641G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600511 | |||||||
chr4:153600686 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2267-1466G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600686 | |||||||
chr4:153600846 | T | C | 70 | a0001c0001t0001g0039 a0001c0001t0002g0061 a0001c0001t0002g0062 others(67): Show |
70 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2267-1306T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153600846 | |||||||
chr4:153600878 | A | AG | 3 | a0001c0003t0001g0117 a0001c0003t0001g0172 a0001c0003t0001g0173 |
3 | NA18981.hp2 NA18983.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2267-1272dupG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr4 | 153600878 | ||||||
chr4:153601107 | C | CA | 59 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0082 others(56): Show |
59 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2267-1029dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr4 | 153601107 | ||||||
chr4:153601107 | C | CAAA | 9 | a0001c0001t0001g0039 a0003c0019t0001g0153 a0003c0019t0001g0154 others(6): Show |
9 | HG01243.hp2 HG01255.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2267-1031_2267-102 others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr4 | 153601107 | ||||||
chr4:153601124 | G | A | 2 | a0001c0004t0001g0193 a0001c0004t0001g0212 |
2 | HG02135.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2267-1028G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153601124 | |||||||
chr4:153601310 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2267-842T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153601310 | |||||||
chr4:153601350 | A | G | 1 | a0001c0014t0001g0211 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2267-802A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153601350 | |||||||
chr4:153601538 | A | C | 1 | a0001c0008t0001g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2267-614A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153601538 | |||||||
chr4:153601605 | G | A | 1 | a0001c0003t0001g0196 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2267-547G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153601605 | |||||||
chr4:153601617 | A | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2267-535A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153601617 | |||||||
chr4:153602002 | A | G | 3 | a0005c0017t0001g0026 a0005c0017t0001g0027 a0005c0017t0001g0040 |
3 | HG02615.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2267-150A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153602002 | |||||||
chr4:153602045 | A | C | 54 | a0002c0006t0001g0118 a0002c0006t0001g0130 a0002c0006t0001g0132 others(51): Show |
54 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.2267-107A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 21/34 | chr4 | 153602045 | |||||||
chr4:153602531 | T | G | 8 | a0003c0019t0001g0153 a0003c0019t0001g0154 a0003c0019t0001g0198 others(5): Show |
8 | HG01255.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2454-11T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 22/34 | chr4 | 153602531 | |||||||
chr4:153602825 | A | C | 2 | a0001c0001t0001g0039 a0001c0024t0001g0015 |
2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2639+98A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 23/34 | chr4 | 153602825 | |||||||
chr4:153602928 | G | A | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2639+201G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 23/34 | chr4 | 153602928 | |||||||
chr4:153603042 | T | C | 1 | a0001c0002t0001g0091 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2640-261T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 23/34 | chr4 | 153603042 | |||||||
chr4:153603481 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0025 |
2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2789+29C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 24/34 | chr4 | 153603481 | |||||||
chr4:153604440 | T | G | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3418+10T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153604440 | |||||||
chr4:153604518 | T | C | 5 | a0002c0006t0001g0202 a0002c0006t0001g0203 a0002c0007t0001g0023 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3418+88T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153604518 | |||||||
chr4:153604698 | T | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0237 others(11): Show |
14 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3418+268T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153604698 | |||||||
chr4:153604784 | G | A | 84 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0039 others(81): Show |
84 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.3418+354G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153604784 | |||||||
chr4:153604796 | C | T | 8 | a0003c0019t0001g0153 a0003c0019t0001g0154 a0003c0019t0001g0198 others(5): Show |
8 | HG01255.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.3418+366C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153604796 | |||||||
chr4:153604837 | T | C | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3418+407T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153604837 | |||||||
chr4:153604893 | C | T | 8 | a0003c0019t0001g0153 a0003c0019t0001g0154 a0003c0019t0001g0198 others(5): Show |
8 | HG01255.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.3418+463C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153604893 | |||||||
chr4:153605048 | T | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0244 a0001c0002t0001g0005 others(7): Show |
10 | HG02055.hp1 HG02486.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3418+618T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605048 | |||||||
chr4:153605058 | A | G | 1 | a0001c0033t0001g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3418+628A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605058 | |||||||
chr4:153605331 | A | G | 1 | a0001c0028t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3418+901A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605331 | |||||||
chr4:153605342 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0039 others(19): Show |
22 | HG01243.hp2 HG01891.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.3418+912C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605342 | |||||||
chr4:153605345 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0024t0001g0015 |
3 | HG02572.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3418+915A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605345 | |||||||
chr4:153605490 | C | G | 10 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0002c0007t0001g0023 others(7): Show |
10 | HG01255.hp1 HG02809.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.3418+1060C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605490 | |||||||
chr4:153605509 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0021t0001g0037 |
3 | HG02572.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3418+1079G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605509 | |||||||
chr4:153605539 | T | C | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3418+1109T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605539 | |||||||
chr4:153605589 | G | C | 3 | a0001c0001t0002g0066 a0001c0005t0002g0064 a0001c0037t0001g0230 |
3 | HG02257.hp1 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3418+1159G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605589 | |||||||
chr4:153605599 | C | T | 11 | a0001c0002t0001g0047 a0001c0002t0001g0245 a0001c0002t0001g0246 others(8): Show |
11 | HG01255.hp1 HG02809.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.3418+1169C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605599 | |||||||
chr4:153605680 | A | G | 1 | a0001c0002t0001g0100 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3418+1250A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605680 | |||||||
chr4:153605738 | T | G | 1 | a0001c0005t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3418+1308T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605738 | |||||||
chr4:153605768 | A | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3418+1338A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605768 | |||||||
chr4:153605954 | T | A | 13 | a0001c0001t0001g0227 a0001c0001t0001g0233 a0001c0001t0001g0236 others(10): Show |
13 | HG02055.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.3418+1524T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605954 | |||||||
chr4:153605974 | GT | G | 3 | a0001c0001t0001g0004 a0001c0001t0002g0061 a0001c0001t0002g0062 |
3 | HG02647.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3418+1545delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153605974 | |||||||
chr4:153606040 | G | A | 3 | a0001c0002t0001g0002 a0005c0017t0001g0026 a0005c0017t0001g0027 |
3 | HG02280.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3418+1610G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153606040 | |||||||
chr4:153606287 | T | G | 34 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0002t0001g0068 others(31): Show |
34 | HG00597.hp1 HG01346.hp2 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.3418+1857T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153606287 | |||||||
chr4:153606360 | A | G | 1 | a0002c0007t0001g0084 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3418+1930A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153606360 | |||||||
chr4:153606463 | A | G | 5 | a0002c0007t0001g0072 a0002c0010t0001g0016 a0002c0029t0001g0067 others(2): Show |
5 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3418+2033A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153606463 | |||||||
chr4:153606806 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3418+2376C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153606806 | |||||||
chr4:153606967 | T | G | 12 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0219 others(9): Show |
12 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3418+2537T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153606967 | |||||||
chr4:153607062 | A | T | 3 | a0002c0025t0001g0103 a0002c0031t0001g0043 a0002c0051t0001g0102 |
3 | NA18950.hp1 NA18986.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3418+2632A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607062 | |||||||
chr4:153607103 | G | T | 129 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(126): Show |
129 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.3418+2673G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607103 | |||||||
chr4:153607165 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3418+2735G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607165 | |||||||
chr4:153607172 | T | A | 2 | a0001c0001t0001g0098 a0001c0024t0001g0015 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3418+2742T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607172 | |||||||
chr4:153607277 | A | G | 2 | a0004c0027t0001g0248 a0004c0036t0001g0234 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3418+2847A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607277 | |||||||
chr4:153607331 | C | T | 177 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(174): Show |
177 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.3418+2901C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607331 | |||||||
chr4:153607465 | C | T | 127 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(124): Show |
127 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.3418+3035C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607465 | |||||||
chr4:153607588 | T | C | 1 | a0001c0005t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3418+3158T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607588 | |||||||
chr4:153607653 | G | T | 3 | a0001c0002t0001g0024 a0001c0002t0002g0065 a0014c0042t0001g0001 |
3 | HG01891.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3418+3223G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607653 | |||||||
chr4:153607668 | A | G | 1 | a0001c0014t0001g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3418+3238A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607668 | |||||||
chr4:153607733 | G | A | 175 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(172): Show |
175 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(172): Show |
intron_variant | MODIFIER | c.3418+3303G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607733 | |||||||
chr4:153607945 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3418+3515A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153607945 | |||||||
chr4:153608448 | C | G | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3419-3804C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153608448 | |||||||
chr4:153608501 | C | T | 6 | a0001c0001t0002g0066 a0001c0005t0001g0106 a0001c0005t0002g0064 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3419-3751C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153608501 | |||||||
chr4:153609048 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3419-3204C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153609048 | |||||||
chr4:153609256 | C | T | 3 | a0001c0002t0001g0024 a0001c0002t0002g0065 a0014c0042t0001g0001 |
3 | HG01891.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3419-2996C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153609256 | |||||||
chr4:153609487 | A | G | 132 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(129): Show |
132 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.3419-2765A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153609487 | |||||||
chr4:153609807 | G | A | 13 | a0001c0002t0001g0047 a0001c0002t0001g0245 a0001c0002t0001g0246 others(10): Show |
13 | HG01123.hp2 HG01255.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.3419-2445G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153609807 | |||||||
chr4:153609865 | T | G | 6 | a0001c0001t0001g0004 a0001c0001t0002g0061 a0001c0001t0002g0062 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3419-2387T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153609865 | |||||||
chr4:153609932 | T | C | 6 | a0001c0001t0002g0066 a0001c0005t0001g0106 a0001c0005t0002g0064 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3419-2320T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153609932 | |||||||
chr4:153610135 | G | C | 1 | a0001c0005t0001g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3419-2117G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610135 | |||||||
chr4:153610150 | T | C | 1 | a0001c0020t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3419-2102T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610150 | |||||||
chr4:153610324 | C | T | 3 | a0001c0003t0001g0119 a0001c0009t0001g0177 a0001c0012t0001g0205 |
3 | HG01496.hp2 HG02004.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3419-1928C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610324 | |||||||
chr4:153610353 | C | A | 1 | a0001c0008t0001g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3419-1899C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610353 | |||||||
chr4:153610512 | A | G | 32 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0002t0001g0068 others(29): Show |
32 | HG00597.hp1 HG01346.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.3419-1740A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610512 | |||||||
chr4:153610536 | G | A | 2 | a0001c0002t0001g0076 a0001c0013t0001g0052 |
2 | NA18942.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.3419-1716G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610536 | |||||||
chr4:153610613 | A | G | 131 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(128): Show |
131 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.3419-1639A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610613 | |||||||
chr4:153610716 | G | GA | 3 | a0001c0002t0001g0045 a0002c0006t0001g0118 a0002c0006t0001g0210 |
3 | NA18953.hp2 NA18994.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.3419-1534dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr4 | 153610716 | ||||||
chr4:153610885 | T | C | 5 | a0001c0001t0001g0227 a0001c0001t0001g0233 a0001c0001t0001g0236 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3419-1367T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610885 | |||||||
chr4:153610895 | G | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(158): Show |
161 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.3419-1357G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610895 | |||||||
chr4:153610898 | T | C | 1 | a0001c0004t0001g0189 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3419-1354T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610898 | |||||||
chr4:153610952 | A | C | 6 | a0003c0019t0001g0153 a0003c0019t0001g0154 a0003c0019t0001g0198 others(3): Show |
6 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.3419-1300A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153610952 | |||||||
chr4:153611155 | G | A | 1 | a0001c0021t0001g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3419-1097G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153611155 | |||||||
chr4:153611198 | G | A | 1 | a0001c0003t0001g0201 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3419-1054G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153611198 | |||||||
chr4:153611309 | G | A | 2 | a0001c0004t0001g0125 a0001c0011t0001g0105 |
2 | HG00140.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.3419-943G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153611309 | |||||||
chr4:153611502 | T | C | 132 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(129): Show |
132 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.3419-750T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153611502 | |||||||
chr4:153611832 | T | C | 1 | a0001c0014t0001g0155 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3419-420T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153611832 | |||||||
chr4:153611835 | A | T | 13 | a0001c0001t0001g0008 a0001c0001t0002g0066 a0001c0002t0001g0024 others(10): Show |
13 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.3419-417A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153611835 | |||||||
chr4:153611904 | G | C | 2 | a0001c0004t0001g0148 a0001c0012t0001g0162 |
2 | NA18955.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.3419-348G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153611904 | |||||||
chr4:153612017 | T | TC | 136 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(133): Show |
136 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.3419-227dupC | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr4 | 153612017 | ||||||
chr4:153612065 | A | G | 1 | a0001c0008t0001g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3419-187A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 25/34 | chr4 | 153612065 | |||||||
chr4:153612449 | C | T | 3 | a0001c0001t0002g0066 a0001c0005t0002g0064 a0001c0037t0001g0230 |
3 | HG02257.hp1 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3567+49C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153612449 | |||||||
chr4:153612669 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0002g0066 others(11): Show |
14 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.3567+269A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153612669 | |||||||
chr4:153612858 | C | T | 2 | a0001c0001t0001g0098 a0001c0024t0001g0015 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3567+458C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153612858 | |||||||
chr4:153612876 | G | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0002g0066 others(30): Show |
33 | HG01123.hp2 HG01255.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.3567+476G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153612876 | |||||||
chr4:153613261 | G | A | 1 | a0001c0011t0001g0110 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3567+861G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153613261 | |||||||
chr4:153613299 | T | C | 1 | a0002c0016t0001g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3567+899T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153613299 | |||||||
chr4:153613361 | A | G | 2 | a0001c0001t0001g0098 a0001c0024t0001g0015 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3567+961A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153613361 | |||||||
chr4:153613665 | A | G | 32 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0002t0001g0068 others(29): Show |
32 | HG00597.hp1 HG01346.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.3567+1265A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153613665 | |||||||
chr4:153613706 | C | T | 1 | a0001c0008t0001g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3567+1306C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153613706 | |||||||
chr4:153613760 | G | T | 1 | a0001c0005t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3567+1360G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153613760 | |||||||
chr4:153613907 | T | C | 2 | a0001c0001t0001g0098 a0001c0024t0001g0015 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3567+1507T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153613907 | |||||||
chr4:153614042 | C | T | 2 | a0002c0007t0001g0071 a0002c0016t0001g0215 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3567+1642C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614042 | |||||||
chr4:153614071 | T | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0002g0066 others(11): Show |
14 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.3567+1671T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614071 | |||||||
chr4:153614082 | G | A | 1 | a0002c0043t0001g0209 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3567+1682G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614082 | |||||||
chr4:153614117 | G | C | 1 | a0001c0009t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3567+1717G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614117 | |||||||
chr4:153614247 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0002c0007t0001g0096 |
3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3567+1847G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614247 | |||||||
chr4:153614298 | G | T | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3567+1898G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614298 | |||||||
chr4:153614421 | G | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0002g0066 others(29): Show |
32 | HG01123.hp2 HG01255.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.3567+2021G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614421 | |||||||
chr4:153614429 | A | G | 1 | a0001c0014t0001g0138 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3567+2029A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614429 | |||||||
chr4:153614636 | A | T | 3 | a0001c0002t0001g0024 a0001c0002t0002g0065 a0014c0042t0001g0001 |
3 | HG01891.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3567+2236A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614636 | |||||||
chr4:153614716 | CA | C | 134 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(131): Show |
134 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.3567+2318delA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr4 | 153614716 | ||||||
chr4:153614812 | A | G | 19 | a0001c0002t0001g0047 a0001c0002t0001g0245 a0001c0002t0001g0246 others(16): Show |
19 | HG01123.hp2 HG01255.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3567+2412A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614812 | |||||||
chr4:153614815 | C | T | 19 | a0001c0002t0001g0047 a0001c0002t0001g0245 a0001c0002t0001g0246 others(16): Show |
19 | HG01123.hp2 HG01255.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3567+2415C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153614815 | |||||||
chr4:153615039 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0219 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3567+2639T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615039 | |||||||
chr4:153615163 | G | A | 19 | a0001c0002t0001g0047 a0001c0002t0001g0245 a0001c0002t0001g0246 others(16): Show |
19 | HG01123.hp2 HG01255.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3567+2763G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615163 | |||||||
chr4:153615298 | A | G | 6 | a0001c0001t0001g0244 a0001c0002t0001g0005 a0001c0002t0002g0080 others(3): Show |
6 | HG02055.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3567+2898A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615298 | |||||||
chr4:153615339 | A | G | 6 | a0001c0001t0001g0244 a0001c0002t0001g0005 a0001c0002t0002g0080 others(3): Show |
6 | HG02055.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3567+2939A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615339 | |||||||
chr4:153615371 | C | T | 1 | a0001c0004t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3567+2971C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615371 | |||||||
chr4:153615372 | G | A | 2 | a0001c0001t0001g0004 a0001c0002t0001g0002 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3567+2972G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615372 | |||||||
chr4:153615572 | G | A | 84 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0041 others(81): Show |
84 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.3567+3172G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615572 | |||||||
chr4:153615578 | T | C | 19 | a0001c0002t0001g0047 a0001c0002t0001g0245 a0001c0002t0001g0246 others(16): Show |
19 | HG01123.hp2 HG01255.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3567+3178T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615578 | |||||||
chr4:153615741 | G | A | 6 | a0003c0019t0001g0153 a0003c0019t0001g0154 a0003c0019t0001g0198 others(3): Show |
6 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.3567+3341G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615741 | |||||||
chr4:153615920 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0002g0066 a0001c0002t0001g0024 others(23): Show |
26 | HG01123.hp2 HG01255.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3567+3520C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615920 | |||||||
chr4:153615922 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3567+3522G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153615922 | |||||||
chr4:153616041 | C | T | 1 | a0001c0005t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3567+3641C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153616041 | |||||||
chr4:153616358 | TTCATTTG others(7): Show |
T | 6 | a0003c0019t0001g0153 a0003c0019t0001g0154 a0003c0019t0001g0198 others(3): Show |
6 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.3567+3964_3567+397 others(18): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr4 | 153616358 | ||||||
chr4:153616529 | C | T | 2 | a0005c0017t0001g0026 a0005c0017t0001g0027 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3567+4129C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153616529 | |||||||
chr4:153616605 | C | T | 2 | a0002c0006t0001g0203 a0002c0007t0001g0023 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3568-4151C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153616605 | |||||||
chr4:153616611 | A | G | 1 | a0001c0037t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3568-4145A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153616611 | |||||||
chr4:153616928 | T | G | 6 | a0003c0019t0001g0153 a0003c0019t0001g0154 a0003c0019t0001g0198 others(3): Show |
6 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.3568-3828T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153616928 | |||||||
chr4:153617093 | A | G | 1 | a0001c0008t0001g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3568-3663A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153617093 | |||||||
chr4:153617182 | G | A | 20 | a0001c0001t0001g0219 a0001c0001t0002g0066 a0001c0002t0001g0005 others(17): Show |
20 | HG01257.hp1 HG01891.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.3568-3574G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153617182 | |||||||
chr4:153617286 | G | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3568-3470G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153617286 | |||||||
chr4:153617476 | C | T | 6 | a0001c0001t0001g0235 a0001c0002t0001g0024 a0001c0008t0001g0204 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3568-3280C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153617476 | |||||||
chr4:153617595 | A | C | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3568-3161A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153617595 | |||||||
chr4:153617718 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3568-3038C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153617718 | |||||||
chr4:153617828 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0235 a0001c0024t0001g0010 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3568-2928T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153617828 | |||||||
chr4:153617863 | G | GT | 52 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0059 others(49): Show |
52 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.3568-2879dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr4 | 153617863 | ||||||
chr4:153617863 | GT | G | 9 | a0001c0002t0001g0047 a0001c0004t0001g0189 a0001c0004t0001g0197 others(6): Show |
9 | HG01255.hp1 HG02886.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.3568-2879delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr4 | 153617863 | ||||||
chr4:153618010 | T | C | 1 | a0004c0018t0001g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3568-2746T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153618010 | |||||||
chr4:153618079 | G | A | 11 | a0001c0001t0001g0219 a0001c0001t0001g0244 a0001c0002t0001g0005 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.3568-2677G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153618079 | |||||||
chr4:153618308 | C | T | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3568-2448C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153618308 | |||||||
chr4:153618476 | C | CA | 25 | a0001c0001t0001g0098 a0001c0001t0001g0225 a0001c0001t0002g0063 others(22): Show |
25 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.3568-2262dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr4 | 153618476 | ||||||
chr4:153618476 | C | CAA | 95 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0042 others(92): Show |
95 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.3568-2263_3568-226 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr4 | 153618476 | ||||||
chr4:153618476 | C | CAAA | 23 | a0001c0001t0001g0039 a0001c0001t0001g0095 a0001c0001t0001g0222 others(20): Show |
23 | HG01123.hp1 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.3568-2264_3568-226 others(7): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr4 | 153618476 | ||||||
chr4:153618698 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3568-2058C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153618698 | |||||||
chr4:153618706 | T | TA | 7 | a0001c0022t0001g0114 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.3568-2049dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr4 | 153618706 | ||||||
chr4:153618904 | T | C | 164 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(161): Show |
164 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.3568-1852T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153618904 | |||||||
chr4:153619022 | A | T | 1 | a0001c0013t0001g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3568-1734A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619022 | |||||||
chr4:153619065 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3568-1691G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619065 | |||||||
chr4:153619098 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3568-1658C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619098 | |||||||
chr4:153619099 | G | A | 5 | a0004c0018t0001g0003 a0004c0018t0001g0101 a0004c0027t0001g0248 others(2): Show |
5 | HG01255.hp1 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3568-1657G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619099 | |||||||
chr4:153619329 | G | A | 1 | a0001c0003t0001g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3568-1427G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619329 | |||||||
chr4:153619335 | A | G | 1 | a0001c0012t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3568-1421A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619335 | |||||||
chr4:153619361 | T | C | 12 | a0001c0001t0001g0086 a0001c0001t0001g0223 a0001c0001t0001g0224 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3568-1395T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619361 | |||||||
chr4:153619378 | C | T | 4 | a0001c0001t0001g0025 a0001c0003t0001g0122 a0001c0003t0001g0124 others(1): Show |
4 | HG01109.hp1 HG01109.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.3568-1378C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619378 | |||||||
chr4:153619434 | G | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3568-1322G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619434 | |||||||
chr4:153619506 | A | G | 7 | a0001c0022t0001g0114 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.3568-1250A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619506 | |||||||
chr4:153619570 | A | G | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3568-1186A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619570 | |||||||
chr4:153619572 | G | A | 1 | a0005c0017t0001g0040 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3568-1184G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619572 | |||||||
chr4:153619591 | T | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(160): Show |
163 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.3568-1165T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619591 | |||||||
chr4:153619749 | C | T | 2 | a0002c0010t0001g0073 a0002c0010t0001g0075 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3568-1007C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619749 | |||||||
chr4:153619825 | G | C | 1 | a0001c0008t0001g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3568-931G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619825 | |||||||
chr4:153619901 | T | A | 159 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(156): Show |
159 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.3568-855T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153619901 | |||||||
chr4:153620001 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0098 others(9): Show |
12 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.3568-755T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153620001 | |||||||
chr4:153620106 | C | T | 1 | a0004c0018t0001g0003 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3568-650C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153620106 | |||||||
chr4:153620144 | T | C | 80 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0039 others(77): Show |
80 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.3568-612T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153620144 | |||||||
chr4:153620167 | T | C | 7 | a0001c0022t0001g0114 a0003c0019t0001g0153 a0003c0019t0001g0154 others(4): Show |
7 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.3568-589T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153620167 | |||||||
chr4:153620196 | T | C | 11 | a0001c0001t0001g0086 a0001c0001t0001g0223 a0001c0001t0001g0224 others(8): Show |
11 | HG01884.hp1 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3568-560T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153620196 | |||||||
chr4:153620197 | G | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(115): Show |
118 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.3568-559G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153620197 | |||||||
chr4:153620553 | C | A | 6 | a0001c0002t0001g0045 a0001c0008t0001g0136 a0001c0011t0001g0050 others(3): Show |
6 | NA18943.hp2 NA18952.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.3568-203C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153620553 | |||||||
chr4:153620591 | C | T | 3 | a0001c0002t0001g0024 a0001c0008t0001g0204 a0014c0042t0001g0001 |
3 | HG01891.hp1 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3568-165C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 26/34 | chr4 | 153620591 | |||||||
chr4:153621009 | C | A | 159 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(156): Show |
159 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.3692+129C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 27/34 | chr4 | 153621009 | |||||||
chr4:153621027 | A | G | 1 | a0003c0019t0001g0153 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3692+147A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 27/34 | chr4 | 153621027 | |||||||
chr4:153621031 | G | A | 1 | a0001c0008t0001g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3692+151G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 27/34 | chr4 | 153621031 | |||||||
chr4:153621417 | G | A | 2 | a0001c0001t0001g0008 a0001c0034t0001g0020 |
2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3693-266G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 27/34 | chr4 | 153621417 | |||||||
chr4:153621457 | T | C | 122 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0025 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.3693-226T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 27/34 | chr4 | 153621457 | |||||||
chr4:153621662 | G | T | 134 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(131): Show |
134 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.3693-21G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 27/34 | chr4 | 153621662 | |||||||
chr4:153621919 | T | C | 9 | a0001c0011t0001g0048 a0001c0022t0001g0078 a0001c0022t0001g0114 others(6): Show |
9 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.3859+70T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153621919 | |||||||
chr4:153621989 | A | G | 2 | a0001c0021t0001g0014 a0002c0007t0001g0096 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3859+140A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153621989 | |||||||
chr4:153622047 | G | A | 1 | a0001c0014t0001g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3859+198G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622047 | |||||||
chr4:153622063 | C | T | 11 | a0001c0011t0001g0048 a0001c0022t0001g0078 a0001c0022t0001g0114 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3859+214C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622063 | |||||||
chr4:153622064 | C | G | 4 | a0001c0002t0001g0024 a0001c0002t0002g0065 a0001c0008t0001g0204 others(1): Show |
4 | HG01891.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3859+215C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622064 | |||||||
chr4:153622093 | C | T | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3859+244C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622093 | |||||||
chr4:153622287 | C | T | 2 | a0002c0007t0001g0070 a0009c0053t0001g0179 |
2 | HG01123.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3859+438C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622287 | |||||||
chr4:153622301 | G | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3859+452G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622301 | |||||||
chr4:153622354 | A | G | 1 | a0001c0034t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3859+505A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622354 | |||||||
chr4:153622405 | A | G | 64 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0089 others(61): Show |
64 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.3860-493A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622405 | |||||||
chr4:153622419 | T | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(95): Show |
98 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.3860-479T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622419 | |||||||
chr4:153622546 | A | C | 8 | a0001c0022t0001g0078 a0001c0022t0001g0114 a0003c0019t0001g0153 others(5): Show |
8 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.3860-352A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622546 | |||||||
chr4:153622619 | T | G | 74 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(71): Show |
74 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.3860-279T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622619 | |||||||
chr4:153622709 | C | T | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3860-189C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622709 | |||||||
chr4:153622843 | A | G | 8 | a0001c0022t0001g0078 a0001c0022t0001g0114 a0003c0019t0001g0153 others(5): Show |
8 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.3860-55A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 28/34 | chr4 | 153622843 | |||||||
chr4:153623114 | C | T | 1 | a0002c0006t0001g0210 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4045+31C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623114 | |||||||
chr4:153623115 | G | A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(128): Show |
131 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.4045+32G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623115 | |||||||
chr4:153623116 | G | T | 2 | a0001c0001t0001g0013 a0001c0024t0001g0010 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4045+33G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623116 | |||||||
chr4:153623174 | G | A | 14 | a0001c0001t0001g0237 a0001c0002t0001g0002 a0001c0002t0001g0019 others(11): Show |
14 | HG01081.hp2 HG01255.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.4045+91G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623174 | |||||||
chr4:153623248 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02486.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4045+165C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623248 | |||||||
chr4:153623295 | A | G | 8 | a0001c0022t0001g0078 a0001c0022t0001g0114 a0003c0019t0001g0153 others(5): Show |
8 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.4045+212A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623295 | |||||||
chr4:153623404 | A | G | 58 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0001t0001g0223 others(55): Show |
58 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.4045+321A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623404 | |||||||
chr4:153623412 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(52): Show |
55 | HG01070.hp1 HG01081.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.4045+329A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623412 | |||||||
chr4:153623453 | A | C | 3 | a0001c0002t0001g0024 a0001c0005t0001g0238 a0014c0042t0001g0001 |
3 | HG01891.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4045+370A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623453 | |||||||
chr4:153623477 | A | G | 1 | a0002c0025t0001g0166 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4045+394A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623477 | |||||||
chr4:153623496 | A | G | 4 | a0001c0002t0001g0024 a0001c0005t0001g0238 a0002c0007t0001g0070 others(1): Show |
4 | HG01891.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4045+413A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623496 | |||||||
chr4:153623594 | A | G | 1 | a0011c0035t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4045+511A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623594 | |||||||
chr4:153623653 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4045+570A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623653 | |||||||
chr4:153623690 | T | G | 1 | a0004c0036t0001g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4045+607T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623690 | |||||||
chr4:153623900 | C | CT | 40 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0002t0001g0047 others(37): Show |
40 | HG00140.hp1 HG00558.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.4045+829dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr4 | 153623900 | ||||||
chr4:153623909 | T | A | 1 | a0002c0039t0001g0053 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4045+826T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623909 | |||||||
chr4:153623912 | T | A | 1 | a0001c0005t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4045+829T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623912 | |||||||
chr4:153623959 | G | C | 1 | a0001c0011t0001g0243 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4045+876G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153623959 | |||||||
chr4:153624067 | T | G | 5 | a0001c0001t0001g0222 a0001c0002t0001g0007 a0001c0005t0001g0232 others(2): Show |
5 | HG02258.hp1 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.4045+984T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624067 | |||||||
chr4:153624104 | G | GT | 45 | a0001c0001t0001g0089 a0001c0001t0001g0223 a0001c0001t0001g0224 others(42): Show |
45 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.4045+1036dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr4 | 153624104 | ||||||
chr4:153624118 | T | C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0237 others(22): Show |
25 | HG01070.hp1 HG01081.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.4045+1035T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624118 | |||||||
chr4:153624128 | A | AT | 40 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0002g0061 others(37): Show |
40 | HG00140.hp1 HG00558.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.4045+1055dupT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr4 | 153624128 | ||||||
chr4:153624128 | A | T | 3 | a0001c0001t0001g0237 a0001c0002t0001g0002 a0001c0005t0003g0034 |
3 | HG02280.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4045+1045A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624128 | |||||||
chr4:153624138 | TGA | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0002t0001g0068 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4045+1063_4045+106 others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr4 | 153624138 | ||||||
chr4:153624299 | A | G | 39 | a0001c0001t0001g0089 a0001c0002t0001g0068 a0001c0002t0001g0076 others(36): Show |
39 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.4045+1216A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624299 | |||||||
chr4:153624366 | G | A | 4 | a0001c0002t0001g0217 a0002c0010t0001g0021 a0004c0018t0001g0029 others(1): Show |
4 | HG02486.hp2 HG02615.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4045+1283G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624366 | |||||||
chr4:153624378 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4045+1295C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624378 | |||||||
chr4:153624410 | C | T | 1 | a0001c0020t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4045+1327C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624410 | |||||||
chr4:153624480 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4045+1397C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624480 | |||||||
chr4:153624584 | A | G | 1 | a0008c0052t0001g0120 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4045+1501A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624584 | |||||||
chr4:153624646 | A | T | 3 | a0001c0001t0001g0098 a0001c0024t0001g0015 a0001c0041t0001g0220 |
3 | HG02258.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4046-1501A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624646 | |||||||
chr4:153624721 | T | G | 3 | a0001c0001t0001g0098 a0001c0024t0001g0015 a0001c0041t0001g0220 |
3 | HG02258.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4046-1426T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624721 | |||||||
chr4:153624951 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0059t0001g0033 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4046-1196C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153624951 | |||||||
chr4:153625140 | A | G | 7 | a0001c0022t0001g0078 a0001c0022t0001g0114 a0003c0019t0001g0153 others(4): Show |
7 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.4046-1007A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625140 | |||||||
chr4:153625174 | G | C | 7 | a0001c0022t0001g0078 a0001c0022t0001g0114 a0003c0019t0001g0153 others(4): Show |
7 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.4046-973G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625174 | |||||||
chr4:153625284 | G | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
37 | HG01081.hp2 HG01255.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4046-863G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625284 | |||||||
chr4:153625450 | A | G | 2 | a0001c0001t0001g0098 a0001c0024t0001g0015 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4046-697A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625450 | |||||||
chr4:153625521 | C | T | 106 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(103): Show |
106 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.4046-626C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625521 | |||||||
chr4:153625549 | T | C | 105 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(102): Show |
105 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.4046-598T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625549 | |||||||
chr4:153625643 | T | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0244 a0001c0005t0001g0038 others(4): Show |
7 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4046-504T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625643 | |||||||
chr4:153625679 | A | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(104): Show |
107 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.4046-468A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625679 | |||||||
chr4:153625772 | G | A | 1 | a0001c0024t0001g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4046-375G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153625772 | |||||||
chr4:153626041 | A | C | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4046-106A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 29/34 | chr4 | 153626041 | |||||||
chr4:153626449 | A | G | 1 | a0003c0023t0001g0083 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4124+224A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626449 | |||||||
chr4:153626454 | G | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
53 | HG01081.hp2 HG01255.hp1 HG01257.hp1 others(50): Show |
intron_variant | MODIFIER | c.4124+229G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626454 | |||||||
chr4:153626465 | A | G | 39 | a0001c0001t0001g0089 a0001c0002t0001g0068 a0001c0002t0001g0076 others(36): Show |
39 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.4124+240A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626465 | |||||||
chr4:153626467 | G | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
53 | HG01081.hp2 HG01255.hp1 HG01257.hp1 others(50): Show |
intron_variant | MODIFIER | c.4124+242G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626467 | |||||||
chr4:153626551 | T | TGGGGGGG others(64): Show |
1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+326_4124+327i others(73): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626551 | |||||||
chr4:153626552 | T | G | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+327T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626552 | |||||||
chr4:153626553 | C | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+328C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626553 | |||||||
chr4:153626558 | C | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+333C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626558 | |||||||
chr4:153626559 | C | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+334C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626559 | |||||||
chr4:153626562 | T | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+337T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626562 | |||||||
chr4:153626563 | C | G | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+338C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626563 | |||||||
chr4:153626564 | T | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+339T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626564 | |||||||
chr4:153626566 | G | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+341G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626566 | |||||||
chr4:153626568 | T | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+343T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626568 | |||||||
chr4:153626569 | A | T | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+344A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626569 | |||||||
chr4:153626573 | T | C | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+348T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626573 | |||||||
chr4:153626574 | AATGAAAC others(57): Show |
A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+350_4124+413d others(66): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626574 | |||||||
chr4:153626629 | C | T | 1 | a0001c0009t0001g0104 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4124+404C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626629 | |||||||
chr4:153626636 | T | C | 103 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
103 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.4124+411T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626636 | |||||||
chr4:153626641 | G | C | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+416G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626641 | |||||||
chr4:153626651 | C | A | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+426C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626651 | |||||||
chr4:153626657 | G | T | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4124+432G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626657 | |||||||
chr4:153626672 | G | T | 39 | a0001c0001t0001g0089 a0001c0002t0001g0068 a0001c0002t0001g0076 others(36): Show |
39 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.4124+447G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626672 | |||||||
chr4:153626788 | A | G | 2 | a0001c0002t0001g0024 a0014c0042t0001g0001 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4124+563A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626788 | |||||||
chr4:153626925 | A | G | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4125-680A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153626925 | |||||||
chr4:153627093 | T | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0095 others(32): Show |
35 | HG01081.hp2 HG01255.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.4125-512T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153627093 | |||||||
chr4:153627196 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0098 others(6): Show |
9 | HG01891.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.4125-409C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153627196 | |||||||
chr4:153627230 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4125-375C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153627230 | |||||||
chr4:153627327 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0008t0001g0204 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4125-278C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153627327 | |||||||
chr4:153627392 | T | C | 3 | a0001c0003t0001g0182 a0001c0011t0001g0110 a0001c0012t0001g0126 |
3 | HG00140.hp2 HG01099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.4125-213T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153627392 | |||||||
chr4:153627393 | G | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0008t0001g0204 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4125-212G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153627393 | |||||||
chr4:153627559 | C | T | 1 | a0001c0002t0001g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4125-46C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153627559 | |||||||
chr4:153627585 | C | T | 1 | a0001c0009t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4125-20C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 30/34 | chr4 | 153627585 | |||||||
chr4:153627700 | C | A | 4 | a0001c0001t0001g0222 a0001c0002t0001g0007 a0001c0005t0001g0232 others(1): Show |
4 | HG02258.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4207+13C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153627700 | |||||||
chr4:153627757 | G | T | 36 | a0001c0001t0001g0008 a0001c0001t0001g0086 a0001c0001t0001g0097 others(33): Show |
36 | HG01081.hp2 HG01255.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.4207+70G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153627757 | |||||||
chr4:153627777 | C | T | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4207+90C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153627777 | |||||||
chr4:153627872 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4207+185G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153627872 | |||||||
chr4:153627908 | C | T | 43 | a0001c0002t0001g0068 a0001c0002t0001g0076 a0001c0002t0001g0091 others(40): Show |
43 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.4207+221C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153627908 | |||||||
chr4:153627932 | C | G | 95 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0025 others(92): Show |
95 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.4207+245C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153627932 | |||||||
chr4:153628003 | A | G | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG02717.hp1 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4207+316A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628003 | |||||||
chr4:153628035 | G | A | 3 | a0001c0002t0001g0005 a0001c0002t0001g0245 a0001c0002t0001g0246 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4207+348G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628035 | |||||||
chr4:153628058 | T | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0086 a0001c0001t0001g0097 others(33): Show |
36 | HG01081.hp2 HG01255.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.4207+371T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628058 | |||||||
chr4:153628158 | A | C | 8 | a0001c0022t0001g0078 a0001c0022t0001g0114 a0003c0019t0001g0153 others(5): Show |
8 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.4207+471A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628158 | |||||||
chr4:153628222 | C | T | 3 | a0001c0002t0001g0217 a0002c0010t0001g0021 a0004c0018t0001g0029 |
3 | HG02486.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4207+535C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628222 | |||||||
chr4:153628469 | T | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0222 a0001c0002t0001g0007 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.4207+782T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628469 | |||||||
chr4:153628511 | T | C | 93 | a0001c0001t0001g0008 a0001c0001t0001g0086 a0001c0001t0001g0089 others(90): Show |
93 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.4207+824T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628511 | |||||||
chr4:153628648 | T | TA | 85 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0058 others(82): Show |
85 | HG00140.hp1 HG01070.hp1 HG01081.hp2 others(82): Show |
intron_variant | MODIFIER | c.4207+968dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr4 | 153628648 | ||||||
chr4:153628652 | A | AC | 6 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0059t0001g0033 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4207+965_4207+966i others(3): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628652 | |||||||
chr4:153628832 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4207+1145G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153628832 | |||||||
chr4:153629010 | C | T | 1 | a0001c0011t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4207+1323C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629010 | |||||||
chr4:153629019 | TGTTACAG others(31): Show |
T | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+1333_4207+137 others(42): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629019 | |||||||
chr4:153629024 | C | T | 4 | a0001c0001t0001g0222 a0001c0002t0001g0007 a0001c0005t0001g0232 others(1): Show |
4 | HG02258.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4207+1337C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629024 | |||||||
chr4:153629040 | T | G | 1 | a0001c0011t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4207+1353T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629040 | |||||||
chr4:153629041 | C | A | 1 | a0001c0011t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4207+1354C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629041 | |||||||
chr4:153629200 | C | G | 1 | a0001c0024t0001g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4207+1513C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629200 | |||||||
chr4:153629228 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0042 others(85): Show |
88 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.4207+1541G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629228 | |||||||
chr4:153629235 | G | A | 15 | a0001c0001t0001g0227 a0001c0001t0001g0237 a0001c0001t0002g0066 others(12): Show |
15 | HG01081.hp2 HG01255.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.4207+1548G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629235 | |||||||
chr4:153629451 | C | T | 61 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0042 others(58): Show |
61 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.4207+1764C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629451 | |||||||
chr4:153629482 | C | T | 22 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0097 others(19): Show |
22 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.4207+1795C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629482 | |||||||
chr4:153629544 | T | C | 31 | a0001c0001t0001g0042 a0001c0002t0001g0068 a0001c0002t0001g0076 others(28): Show |
31 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.4207+1857T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629544 | |||||||
chr4:153629573 | C | A | 62 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(59): Show |
62 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(59): Show |
intron_variant | MODIFIER | c.4207+1886C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629573 | |||||||
chr4:153629677 | G | T | 62 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(59): Show |
62 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(59): Show |
intron_variant | MODIFIER | c.4207+1990G>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629677 | |||||||
chr4:153629868 | C | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0098 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4207+2181C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629868 | |||||||
chr4:153629960 | A | G | 67 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(64): Show |
67 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(64): Show |
intron_variant | MODIFIER | c.4207+2273A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153629960 | |||||||
chr4:153630087 | T | TGGGGGGG others(27): Show |
1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2401_4207+240 others(38): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr4 | 153630087 | ||||||
chr4:153630089 | C | G | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2402C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630089 | |||||||
chr4:153630092 | C | G | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2405C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630092 | |||||||
chr4:153630094 | C | T | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2407C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630094 | |||||||
chr4:153630095 | A | G | 67 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(64): Show |
67 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(64): Show |
intron_variant | MODIFIER | c.4207+2408A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630095 | |||||||
chr4:153630096 | T | C | 1 | a0004c0018t0001g0003 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4207+2409T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630096 | |||||||
chr4:153630103 | C | G | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2416C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630103 | |||||||
chr4:153630105 | C | T | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2418C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630105 | |||||||
chr4:153630108 | A | G | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2421A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630108 | |||||||
chr4:153630109 | A | G | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2422A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630109 | |||||||
chr4:153630111 | C | T | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2424C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630111 | |||||||
chr4:153630112 | C | T | 1 | a0001c0004t0001g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4207+2425C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630112 | |||||||
chr4:153630131 | T | C | 26 | a0001c0001t0001g0025 a0001c0001t0001g0219 a0001c0001t0001g0222 others(23): Show |
26 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.4207+2444T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630131 | |||||||
chr4:153630194 | G | A | 1 | a0002c0007t0001g0084 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4207+2507G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630194 | |||||||
chr4:153630226 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0098 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4208-2492G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630226 | |||||||
chr4:153630322 | T | C | 7 | a0001c0022t0001g0078 a0001c0022t0001g0114 a0003c0019t0001g0153 others(4): Show |
7 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.4208-2396T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630322 | |||||||
chr4:153630666 | A | T | 1 | a0002c0045t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4208-2052A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630666 | |||||||
chr4:153630741 | C | T | 3 | a0002c0006t0001g0164 a0002c0006t0001g0186 a0002c0015t0001g0018 |
3 | NA18978.hp2 NA18981.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.4208-1977C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630741 | |||||||
chr4:153630787 | AC | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0002g0082 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.4208-1928delC | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr4 | 153630787 | ||||||
chr4:153630832 | G | A | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG02717.hp1 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4208-1886G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630832 | |||||||
chr4:153630851 | C | T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0039 others(37): Show |
40 | HG01243.hp2 HG01257.hp1 HG01516.hp2 others(37): Show |
intron_variant | MODIFIER | c.4208-1867C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153630851 | |||||||
chr4:153630997 | C | CA | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0002t0001g0009 |
3 | HG02647.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4208-1719dupA | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr4 | 153630997 | ||||||
chr4:153631047 | G | A | 1 | a0001c0041t0001g0220 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4208-1671G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631047 | |||||||
chr4:153631053 | T | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(139): Show |
142 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.4208-1665T>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631053 | |||||||
chr4:153631068 | G | A | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4208-1650G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631068 | |||||||
chr4:153631099 | C | T | 1 | a0001c0004t0001g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4208-1619C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631099 | |||||||
chr4:153631115 | G | A | 1 | a0001c0009t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4208-1603G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631115 | |||||||
chr4:153631458 | TCAGA | T | 27 | a0001c0001t0001g0025 a0001c0001t0001g0219 a0001c0001t0001g0222 others(24): Show |
27 | HG02055.hp1 HG02135.hp2 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.4208-1256_4208-125 others(8): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr4 | 153631458 | ||||||
chr4:153631470 | A | G | 1 | a0002c0007t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4208-1248A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631470 | |||||||
chr4:153631532 | A | G | 1 | a0001c0009t0001g0190 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.4208-1186A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631532 | |||||||
chr4:153631714 | A | G | 22 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0097 others(19): Show |
22 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.4208-1004A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631714 | |||||||
chr4:153631867 | A | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0245 a0001c0002t0001g0246 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4208-851A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153631867 | |||||||
chr4:153632101 | C | T | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4208-617C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153632101 | |||||||
chr4:153632124 | T | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(144): Show |
147 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.4208-594T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153632124 | |||||||
chr4:153632204 | G | A | 8 | a0001c0001t0001g0013 a0001c0002t0001g0024 a0001c0002t0001g0217 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.4208-514G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153632204 | |||||||
chr4:153632310 | C | T | 56 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0001g0219 others(53): Show |
56 | HG00140.hp1 HG00597.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.4208-408C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153632310 | |||||||
chr4:153632311 | T | TC | 7 | a0001c0002t0001g0024 a0001c0002t0001g0217 a0002c0010t0001g0021 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.4208-401dupC | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr4 | 153632311 | ||||||
chr4:153632541 | G | A | 106 | a0001c0001t0001g0041 a0001c0001t0001g0059 a0001c0001t0001g0089 others(103): Show |
106 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.4208-177G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153632541 | |||||||
chr4:153632562 | T | G | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG02717.hp1 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4208-156T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153632562 | |||||||
chr4:153632681 | A | G | 30 | a0001c0001t0001g0058 a0001c0002t0001g0047 a0001c0003t0001g0163 others(27): Show |
30 | HG00140.hp1 HG00597.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.4208-37A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 31/34 | chr4 | 153632681 | |||||||
chr4:153633031 | TAAAA | T | 60 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0039 others(57): Show |
60 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.4328+194_4328+197d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633031 | |||||||
chr4:153633069 | A | T | 2 | a0001c0001t0002g0062 a0001c0002t0001g0009 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4328+231A>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633069 | |||||||
chr4:153633088 | A | G | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4328+250A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633088 | |||||||
chr4:153633090 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4328+252G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633090 | |||||||
chr4:153633108 | A | G | 1 | a0001c0012t0001g0126 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4328+270A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633108 | |||||||
chr4:153633202 | G | A | 1 | a0001c0009t0001g0190 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.4328+364G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633202 | |||||||
chr4:153633214 | CGTTT | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0039 others(58): Show |
61 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.4328+381_4328+384d others(6): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr4 | 153633214 | ||||||
chr4:153633320 | G | A | 102 | a0001c0001t0001g0041 a0001c0001t0001g0059 a0001c0001t0001g0089 others(99): Show |
102 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.4328+482G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633320 | |||||||
chr4:153633321 | G | A | 2 | a0001c0002t0001g0024 a0014c0042t0001g0001 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4328+483G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633321 | |||||||
chr4:153633343 | A | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0222 a0001c0001t0002g0063 others(9): Show |
12 | HG01255.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.4328+505A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633343 | |||||||
chr4:153633359 | G | A | 20 | a0001c0001t0001g0025 a0001c0001t0001g0219 a0001c0001t0001g0222 others(17): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.4328+521G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633359 | |||||||
chr4:153633390 | AT | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(170): Show |
173 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.4328+571delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr4 | 153633390 | ||||||
chr4:153633466 | C | G | 6 | a0001c0001t0001g0013 a0001c0002t0001g0217 a0002c0010t0001g0021 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4328+628C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633466 | |||||||
chr4:153633506 | G | A | 33 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0095 others(30): Show |
33 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.4328+668G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633506 | |||||||
chr4:153633855 | C | T | 2 | a0001c0002t0001g0024 a0014c0042t0001g0001 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4329-337C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633855 | |||||||
chr4:153633901 | C | T | 19 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0097 others(16): Show |
19 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.4329-291C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633901 | |||||||
chr4:153633982 | G | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0098 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4329-210G>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633982 | |||||||
chr4:153633985 | C | T | 1 | a0003c0019t0001g0154 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4329-207C>T | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153633985 | |||||||
chr4:153634036 | C | A | 1 | a0001c0002t0001g0217 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4329-156C>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 32/34 | chr4 | 153634036 | |||||||
chr4:153634284 | AG | A | 6 | a0001c0001t0001g0086 a0001c0001t0001g0097 a0001c0002t0002g0080 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG03540.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.4417+7delG | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr4 | 153634284 | ||||||
chr4:153634378 | A | G | 1 | a0002c0007t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4417+98A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 33/34 | chr4 | 153634378 | |||||||
chr4:153634587 | T | C | 1 | a0002c0007t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4417+307T>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 33/34 | chr4 | 153634587 | |||||||
chr4:153634789 | A | C | 1 | a0004c0018t0001g0003 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4417+509A>C | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 33/34 | chr4 | 153634789 | |||||||
chr4:153634943 | A | G | 1 | a0006c0040t0001g0030 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4418-489A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 33/34 | chr4 | 153634943 | |||||||
chr4:153635027 | G | A | 3 | a0001c0002t0001g0060 a0001c0005t0001g0109 a0001c0008t0001g0199 |
3 | HG01109.hp2 HG01192.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.4418-405G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 33/34 | chr4 | 153635027 | |||||||
chr4:153635120 | A | G | 2 | a0001c0005t0001g0238 a0001c0041t0001g0220 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.4418-312A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 33/34 | chr4 | 153635120 | |||||||
chr4:153635275 | A | G | 16 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0223 others(13): Show |
16 | HG02055.hp2 HG02486.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.4418-157A>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 33/34 | chr4 | 153635275 | |||||||
chr4:153635646 | C | G | 171 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(168): Show |
171 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.4557+75C>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 34/34 | chr4 | 153635646 | |||||||
chr4:153635662 | G | A | 2 | a0001c0002t0001g0024 a0014c0042t0001g0001 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4557+91G>A | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 34/34 | chr4 | 153635662 | |||||||
chr4:153635759 | T | G | 7 | a0001c0022t0001g0078 a0001c0022t0001g0114 a0003c0019t0001g0153 others(4): Show |
7 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.4557+188T>G | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 34/34 | chr4 | 153635759 | |||||||
chr4:153636231 | ATG | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(165): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.4558-66_4558-65del others(2): Show |
TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr4 | 153636231 | ||||||
chr4:153636253 | CT | C | 168 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(165): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.4558-38delT | TMEM131L | ENSG00000121210.16 | transcript | ENST00000409959.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr4 | 153636253 |