Item | Value |
---|---|
geneid | 6597 |
ensemblid | ENSG00000127616.22 |
hgncid | 11100 |
symbol | SMARCA4 |
name | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 |
refseq_nuc | NM_003072.5 |
refseq_prot | NP_003063.2 |
ensembl_nuc | ENST00000344626.10 |
ensembl_prot | ENSP00000343896.4 |
mane_status | MANE Select |
chr | chr19 |
start | 10961030 |
end | 11062273 |
strand | + |
ver | v1.2 |
region | chr19:10961030-11062273 |
region5000 | chr19:10956030-11067273 |
regionname0 | SMARCA4_chr19_10961030_11062273 |
regionname5000 | SMARCA4_chr19_10956030_11067273 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1647 | 282 | 69 | 47 | 117 | 9 | 38 | 87 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | MSTPD others(1642): Show |
chr19 | 10956030 | 11067273 |
a0002 | 0/0 | 1647 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | MSTPD others(1642): Show |
chr19 | 10956030 | 11067273 |
a0003 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | MSTPD others(1642): Show |
chr19 | 10956030 | 11067273 |
a0004 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | MSTPD others(1642): Show |
chr19 | 10956030 | 11067273 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4941 | 145 | 25 | 27 | 73 | 4 | 14 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0002 | 0/0 | 4941 | 39 | 5 | 7 | 25 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0003 | 0/0 | 4941 | 31 | 2 | 7 | 9 | 4 | 9 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0004 | 0/0 | 4941 | 18 | 14 | 0 | 3 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0005 | 0/0 | 4941 | 5 | 5 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0006 | 0/0 | 4941 | 4 | 4 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0007 | 0/0 | 4941 | 4 | 0 | 1 | 2 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0008 | 0/0 | 4941 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0009 | 0/0 | 4941 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0010 | 0/0 | 4941 | 3 | 0 | 3 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0011 | 0/0 | 4941 | 3 | 0 | 0 | 0 | 0 | 3 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0012 | 0/0 | 4941 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0014 | 0/0 | 4941 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0015 | 0/0 | 4941 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0016 | 0/0 | 4941 | 2 | 2 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0017 | 0/0 | 4941 | 2 | 1 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0018 | 0/0 | 4941 | 2 | 0 | 0 | 2 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0019 | 0/0 | 4941 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0020 | 0/0 | 4941 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0021 | 0/0 | 4941 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0022 | 0/0 | 4941 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0024 | 0/0 | 4941 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0025 | 0/0 | 4941 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0026 | 0/0 | 4941 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0027 | 0/0 | 4941 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0028 | 0/0 | 4941 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0030 | 0/0 | 4941 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0031 | 0/0 | 4941 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0001c0032 | 0/0 | 4941 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0002c0013 | 0/0 | 4941 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0003c0023 | 0/0 | 4941 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 | ||
a0004c0029 | 0/0 | 4941 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | ATGTC others(4936): Show |
chr19 | 10956030 | 11067273 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5577 | 143 | 25 | 26 | 72 | 4 | 14 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0001t0002 | 0/0 | 5577 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0001t0004 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0002t0001 | 0/0 | 5577 | 39 | 5 | 7 | 25 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0003t0001 | 0/0 | 5577 | 31 | 2 | 7 | 9 | 4 | 9 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0004t0001 | 0/0 | 5577 | 17 | 13 | 0 | 3 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0004t0003 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0005t0001 | 0/0 | 5577 | 5 | 5 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0006t0001 | 0/0 | 5577 | 4 | 4 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0007t0001 | 0/0 | 5577 | 4 | 0 | 1 | 2 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0008t0001 | 0/0 | 5577 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0009t0001 | 0/0 | 5577 | 3 | 3 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0010t0001 | 0/0 | 5577 | 3 | 0 | 3 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0011t0001 | 0/0 | 5577 | 3 | 0 | 0 | 0 | 0 | 3 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0012t0001 | 0/0 | 5577 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0014t0001 | 0/0 | 5577 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0015t0001 | 0/0 | 5577 | 2 | 0 | 0 | 0 | 0 | 2 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0016t0001 | 0/0 | 5577 | 2 | 2 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0017t0001 | 0/0 | 5577 | 2 | 1 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0018t0001 | 0/0 | 5577 | 2 | 0 | 0 | 2 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0019t0001 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0020t0001 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0021t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0022t0001 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0024t0001 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0025t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0026t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0027t0001 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0028t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0030t0001 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0031t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0001c0032t0001 | 0/0 | 5577 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0002c0013t0001 | 0/0 | 5577 | 2 | 0 | 1 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0003c0023t0001 | 0/0 | 5577 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
a0004c0029t0001 | 0/0 | 5577 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | GGGCG others(5572): Show |
chr19 | 10956030 | 11067273 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0004t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0005t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0006t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0007t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0007t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0007t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0007t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0008t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0008t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0008t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0009t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0009t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0009t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0010t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0010t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0010t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0011t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0011t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0011t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0012t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0012t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0014t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0014t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0015t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0015t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0016t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0016t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0017t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0017t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0018t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0018t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0019t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0020t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0021t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0022t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0024t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0025t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0026t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0027t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0028t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0030t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0031t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0001c0032t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0002c0013t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0002c0013t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0003c0023t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
a0004c0029t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0227 | EUR | GBR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00639 | hp2 | a0001 | c0014 | t0001 | g0235 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01069 | hp1 | a0001 | c0010 | t0001 | g0009 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01071 | hp2 | a0001 | c0010 | t0001 | g0010 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0221 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01109 | hp1 | a0001 | c0017 | t0001 | g0031 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01168 | hp2 | a0001 | c0003 | t0001 | g0260 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | PUR | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01255 | hp1 | a0002 | c0013 | t0001 | g0020 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0244 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0206 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01358 | hp1 | a0001 | c0010 | t0001 | g0011 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01515 | hp2 | a0001 | c0014 | t0001 | g0233 | EUR | IBS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0209 | EUR | IBS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01516 | hp2 | a0002 | c0013 | t0001 | g0016 | EUR | IBS | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01884 | hp2 | a0001 | c0005 | t0001 | g0242 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0216 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01981 | hp1 | a0001 | c0007 | t0001 | g0019 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0181 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02055 | hp2 | a0001 | c0005 | t0001 | g0262 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02071 | hp2 | a0001 | c0007 | t0001 | g0018 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02083 | hp1 | a0001 | c0030 | t0001 | g0212 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02083 | hp2 | a0001 | c0004 | t0001 | g0079 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02135 | hp2 | a0001 | c0007 | t0001 | g0021 | EAS | KHV | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02145 | hp1 | a0001 | c0004 | t0001 | g0160 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0025 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0139 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02280 | hp2 | a0001 | c0008 | t0001 | g0268 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02622 | hp1 | a0001 | c0004 | t0001 | g0191 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02630 | hp1 | a0001 | c0009 | t0001 | g0003 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02647 | hp1 | a0001 | c0004 | t0001 | g0140 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0149 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02698 | hp1 | a0001 | c0011 | t0001 | g0276 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02698 | hp2 | a0001 | c0015 | t0001 | g0023 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0178 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02735 | hp2 | a0001 | c0007 | t0001 | g0017 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02738 | hp2 | a0001 | c0011 | t0001 | g0278 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02809 | hp1 | a0001 | c0006 | t0001 | g0271 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02809 | hp2 | a0003 | c0023 | t0001 | g0004 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02896 | hp2 | a0001 | c0006 | t0001 | g0272 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0128 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02897 | hp2 | a0001 | c0006 | t0001 | g0270 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02922 | hp2 | a0001 | c0028 | t0001 | g0007 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02965 | hp1 | a0001 | c0016 | t0001 | g0228 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02970 | hp1 | a0001 | c0016 | t0001 | g0230 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03041 | hp1 | a0001 | c0009 | t0001 | g0001 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03041 | hp2 | a0001 | c0008 | t0001 | g0266 | AFR | GWD | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0243 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03098 | hp2 | a0001 | c0004 | t0001 | g0082 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03130 | hp1 | a0001 | c0021 | t0001 | g0175 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03139 | hp1 | a0001 | c0017 | t0001 | g0183 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0121 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03195 | hp2 | a0001 | c0005 | t0001 | g0256 | AFR | ESN | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03239 | hp1 | a0001 | c0004 | t0001 | g0005 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0237 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0083 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0273 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03491 | hp1 | a0001 | c0012 | t0001 | g0013 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03492 | hp1 | a0001 | c0012 | t0001 | g0015 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0159 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0211 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03669 | hp2 | a0001 | c0027 | t0001 | g0014 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03704 | hp1 | a0001 | c0032 | t0001 | g0231 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03704 | hp2 | a0001 | c0020 | t0001 | g0234 | SAS | PJL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03831 | hp1 | a0001 | c0015 | t0001 | g0022 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0210 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03942 | hp1 | a0001 | c0011 | t0001 | g0277 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0248 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0241 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0204 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG04204 | hp2 | a0001 | c0024 | t0001 | g0012 | SAS | STU | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18522 | hp1 | a0001 | c0004 | t0003 | g0180 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18522 | hp2 | a0001 | c0031 | t0001 | g0008 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18906 | hp2 | a0001 | c0008 | t0001 | g0269 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18940 | hp1 | a0001 | c0018 | t0001 | g0039 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18979 | hp1 | a0001 | c0019 | t0001 | g0192 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18983 | hp1 | a0004 | c0029 | t0001 | g0051 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18985 | hp1 | a0001 | c0003 | t0001 | g0249 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA18997 | hp2 | a0001 | c0018 | t0001 | g0157 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19000 | hp1 | a0001 | c0004 | t0001 | g0185 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | LWK | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | LWK | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19043 | hp2 | a0001 | c0004 | t0001 | g0167 | AFR | LWK | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19058 | hp2 | a0001 | c0022 | t0001 | g0201 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19060 | hp2 | a0001 | c0004 | t0001 | g0071 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0258 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19240 | hp1 | a0001 | c0004 | t0001 | g0138 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA20129 | hp1 | a0001 | c0026 | t0001 | g0281 | AFR | ASW | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA20129 | hp2 | a0001 | c0025 | t0001 | g0040 | AFR | ASW | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0225 | EUR | TSI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0137 | EUR | TSI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02109 | hp1 | a0001 | c0006 | t0001 | g0267 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02109 | hp2 | a0001 | c0005 | t0001 | g0078 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02559 | hp1 | a0001 | c0009 | t0001 | g0002 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | USA | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0109 | REF | REF | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0108 | REF | REF | SMARCA4_chr19_10956030_11067273 | SMARCA4 | chr19 | 10956030 | 11067273 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:10986435 | A | T | 1 | a0004 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.602A>T | p.Gln201Leu | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/35 | 778/5577 | 602/4944 | 201/1647 | chr19 | 10986435 | |||
chr19:10987920 | T | C | 1 | a0002 | 2 | HG01255.hp1 HG01516.hp2 |
missense_variant | MODERATE | c.1114T>C | p.Tyr372His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/35 | 1290/5577 | 1114/4944 | 372/1647 | chr19 | 10987920 | |||
chr19:11059885 | T | A | 1 | a0003 | 1 | HG02809.hp2 | missense_variant&splice_region_variant | MODERATE | c.4768T>A | p.Ser1590Thr | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/35 | 4944/5577 | 4768/4944 | 1590/1647 | chr19 | 11059885 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:10984205 | G | A | 1 | a0001c0012 | 2 | HG03491.hp1 HG03492.hp1 |
synonymous_variant | LOW | c.54G>A | p.Pro18Pro | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/35 | 230/5577 | 54/4944 | 18/1647 | chr19 | 10984205 | |||
chr19:10984271 | C | T | 1 | a0001c0032 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.120C>T | p.His40His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/35 | 296/5577 | 120/4944 | 40/1647 | chr19 | 10984271 | |||
chr19:10985308 | C | T | 1 | a0001c0031 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.258C>T | p.Asp86Asp | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/35 | 434/5577 | 258/4944 | 86/1647 | chr19 | 10985308 | |||
chr19:10986424 | C | T | 1 | a0001c0030 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.591C>T | p.Pro197Pro | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/35 | 767/5577 | 591/4944 | 197/1647 | chr19 | 10986424 | |||
chr19:10987721 | G | A | 2 | a0001c0006 a0001c0008 |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.915G>A | p.Pro305Pro | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/35 | 1091/5577 | 915/4944 | 305/1647 | chr19 | 10987721 | |||
chr19:10987736 | C | A | 1 | a0001c0005 | 5 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
synonymous_variant | LOW | c.930C>A | p.Arg310Arg | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/35 | 1106/5577 | 930/4944 | 310/1647 | chr19 | 10987736 | |||
chr19:10989338 | C | T | 1 | a0001c0028 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1140C>T | p.His380His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/35 | 1316/5577 | 1140/4944 | 380/1647 | chr19 | 10989338 | |||
chr19:10989407 | G | A | 1 | a0001c0019 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1209G>A | p.Glu403Glu | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/35 | 1385/5577 | 1209/4944 | 403/1647 | chr19 | 10989407 | |||
chr19:10991317 | G | A | 2 | a0001c0009 a0001c0010 |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
synonymous_variant | LOW | c.1413G>A | p.Lys471Lys | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/35 | 1589/5577 | 1413/4944 | 471/1647 | chr19 | 10991317 | |||
chr19:10994917 | A | G | 1 | a0001c0010 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
synonymous_variant | LOW | c.1509A>G | p.Ala503Ala | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/35 | 1685/5577 | 1509/4944 | 503/1647 | chr19 | 10994917 | |||
chr19:10994932 | T | C | 18 | a0001c0002 a0001c0003 a0001c0005 others(15): Show |
107 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
synonymous_variant | LOW | c.1524T>C | p.His508His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/35 | 1700/5577 | 1524/4944 | 508/1647 | chr19 | 10994932 | |||
chr19:10994965 | C | T | 1 | a0001c0018 | 2 | NA18940.hp1 NA18997.hp2 |
synonymous_variant | LOW | c.1557C>T | p.Asn519Asn | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/35 | 1733/5577 | 1557/4944 | 519/1647 | chr19 | 10994965 | |||
chr19:10996359 | A | G | 1 | a0001c0016 | 2 | HG02965.hp1 HG02970.hp1 |
synonymous_variant | LOW | c.1740A>G | p.Lys580Lys | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 10/35 | 1916/5577 | 1740/4944 | 580/1647 | chr19 | 10996359 | |||
chr19:11013062 | C | T | 2 | a0001c0011 a0001c0027 |
4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
synonymous_variant | LOW | c.2388C>T | p.Leu796Leu | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/35 | 2564/5577 | 2388/4944 | 796/1647 | chr19 | 11013062 | |||
chr19:11021958 | C | T | 1 | a0001c0026 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2850C>T | p.Thr950Thr | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/35 | 3026/5577 | 2850/4944 | 950/1647 | chr19 | 11021958 | |||
chr19:11024423 | C | T | 1 | a0001c0020 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.3066C>T | p.Ser1022Ser | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/35 | 3242/5577 | 3066/4944 | 1022/1647 | chr19 | 11024423 | |||
chr19:11033406 | G | A | 1 | a0001c0021 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.3663G>A | p.Lys1221Lys | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 26/35 | 3839/5577 | 3663/4944 | 1221/1647 | chr19 | 11033406 | |||
chr19:11034176 | C | T | 1 | a0001c0025 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.3927C>T | p.His1309His | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/35 | 4103/5577 | 3927/4944 | 1309/1647 | chr19 | 11034176 | |||
chr19:11035015 | C | T | 4 | a0001c0007 a0001c0012 a0001c0015 others(1): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
synonymous_variant | LOW | c.4053C>T | p.Asp1351Asp | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/35 | 4229/5577 | 4053/4944 | 1351/1647 | chr19 | 11035015 | |||
chr19:11041363 | A | G | 1 | a0001c0021 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.4227A>G | p.Ser1409Ser | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/35 | 4403/5577 | 4227/4944 | 1409/1647 | chr19 | 11041363 | |||
chr19:11058324 | C | T | 1 | a0001c0017 | 2 | HG01109.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.4494C>T | p.Tyr1498Tyr | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/35 | 4670/5577 | 4494/4944 | 1498/1647 | chr19 | 11058324 | |||
chr19:11058838 | C | T | 4 | a0001c0014 a0001c0015 a0001c0020 others(1): Show |
6 | HG00639.hp2 HG01515.hp2 HG02698.hp2 others(3): Show |
synonymous_variant | LOW | c.4584C>T | p.Asp1528Asp | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/35 | 4760/5577 | 4584/4944 | 1528/1647 | chr19 | 11058838 | |||
chr19:11059812 | G | A | 1 | a0001c0022 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.4695G>A | p.Glu1565Glu | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/35 | 4871/5577 | 4695/4944 | 1565/1647 | chr19 | 11059812 | |||
chr19:11060163 | T | C | 13 | a0001c0003 a0001c0004 a0001c0008 others(10): Show |
69 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(66): Show |
synonymous_variant | LOW | c.4887T>C | p.Asp1629Asp | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/35 | 5063/5577 | 4887/4944 | 1629/1647 | chr19 | 11060163 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:10961061 | C | T | 1 | a0001c0001t0004 | 1 | NA18957.hp2 | 5_prime_UTR_variant | MODIFIER | c.-145C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/35 | 23091 | chr19 | 10961061 | ||||||
chr19:11061817 | G | T | 1 | a0001c0004t0003 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 35/35 | 1 | chr19 | 11061817 | ||||||
chr19:11062102 | A | G | 1 | a0001c0001t0002 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 35/35 | 286 | chr19 | 11062102 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:10961242 | G | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+68G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961242 | |||||||
chr19:10961250 | G | C | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-32+76G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961250 | |||||||
chr19:10961336 | G | T | 1 | a0001c0001t0001g0286 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-32+162G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961336 | |||||||
chr19:10961337 | T | G | 1 | a0001c0001t0001g0286 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-32+163T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961337 | |||||||
chr19:10961458 | G | T | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(1): Show |
4 | NA18947.hp1 NA18957.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32+284G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961458 | |||||||
chr19:10961516 | C | T | 89 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(86): Show |
89 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.-32+342C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961516 | |||||||
chr19:10961539 | C | G | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+365C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961539 | |||||||
chr19:10961560 | G | C | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-32+386G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961560 | |||||||
chr19:10961596 | C | G | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-32+422C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961596 | |||||||
chr19:10961647 | C | T | 1 | a0001c0002t0001g0279 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-32+473C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961647 | |||||||
chr19:10961674 | G | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+500G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961674 | |||||||
chr19:10961713 | C | T | 1 | a0001c0019t0001g0192 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-32+539C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961713 | |||||||
chr19:10961768 | A | G | 4 | a0001c0001t0001g0275 a0001c0011t0001g0276 a0001c0011t0001g0277 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32+594A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961768 | |||||||
chr19:10961802 | T | C | 24 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0003t0001g0006 others(21): Show |
24 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-32+628T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961802 | |||||||
chr19:10961934 | G | A | 112 | a0001c0001t0001g0024 a0001c0001t0001g0193 a0001c0001t0001g0194 others(109): Show |
112 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.-32+760G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10961934 | |||||||
chr19:10961972 | A | AT | 36 | a0001c0001t0001g0026 a0001c0001t0001g0179 a0001c0001t0001g0182 others(33): Show |
36 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32+818dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10961972 | ||||||
chr19:10961972 | A | ATT | 13 | a0001c0001t0001g0024 a0001c0004t0001g0025 a0001c0007t0001g0017 others(10): Show |
13 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32+817_-32+818dup others(2): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10961972 | ||||||
chr19:10962310 | A | G | 1 | a0001c0003t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-32+1136A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962310 | |||||||
chr19:10962325 | CCTA | C | 13 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(10): Show |
13 | HG01081.hp1 HG01167.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32+1155_-32+1157d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10962325 | ||||||
chr19:10962541 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | HG02451.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+1367G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962541 | |||||||
chr19:10962657 | C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-32+1483C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962657 | |||||||
chr19:10962694 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-32+1520C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962694 | |||||||
chr19:10962764 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-32+1590A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10962764 | |||||||
chr19:10962804 | AAGTGCT | A | 12 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(9): Show |
12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+1633_-32+1638d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10962804 | ||||||
chr19:10963178 | A | T | 1 | a0001c0005t0001g0262 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-32+2004A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963178 | |||||||
chr19:10963245 | C | T | 1 | a0001c0024t0001g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-32+2071C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963245 | |||||||
chr19:10963361 | A | T | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-32+2187A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963361 | |||||||
chr19:10963370 | C | CA | 31 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(28): Show |
31 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-32+2217dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10963370 | ||||||
chr19:10963370 | CA | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0173 a0001c0002t0001g0174 others(6): Show |
9 | HG01168.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32+2217delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10963370 | ||||||
chr19:10963396 | A | G | 2 | a0001c0010t0001g0010 a0001c0010t0001g0011 |
2 | HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-32+2222A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963396 | |||||||
chr19:10963441 | G | A | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-32+2267G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963441 | |||||||
chr19:10963467 | T | G | 2 | a0001c0017t0001g0031 a0001c0017t0001g0183 |
2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-32+2293T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963467 | |||||||
chr19:10963606 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-32+2432G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963606 | |||||||
chr19:10963753 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32+2579G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10963753 | |||||||
chr19:10963767 | A | AT | 33 | a0001c0001t0001g0024 a0001c0001t0001g0171 a0001c0002t0001g0207 others(30): Show |
33 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-32+2609dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10963767 | ||||||
chr19:10963767 | A | ATT | 80 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(77): Show |
80 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-32+2608_-32+2609d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10963767 | ||||||
chr19:10964253 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-32+3079G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964253 | |||||||
chr19:10964321 | T | C | 6 | a0001c0003t0001g0006 a0001c0010t0001g0009 a0001c0010t0001g0010 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+3147T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964321 | |||||||
chr19:10964626 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG00408.hp1 NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-32+3452T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964626 | |||||||
chr19:10964632 | T | C | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+3458T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964632 | |||||||
chr19:10964636 | A | T | 114 | a0001c0001t0001g0024 a0001c0001t0001g0193 a0001c0001t0001g0194 others(111): Show |
114 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-32+3462A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964636 | |||||||
chr19:10964691 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-32+3517C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964691 | |||||||
chr19:10964738 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-32+3564C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964738 | |||||||
chr19:10964837 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32+3663T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964837 | |||||||
chr19:10964884 | G | A | 42 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0044 others(39): Show |
42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.-32+3710G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964884 | |||||||
chr19:10964910 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-32+3736C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10964910 | |||||||
chr19:10965030 | A | G | 166 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(163): Show |
166 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-32+3856A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965030 | |||||||
chr19:10965073 | C | T | 10 | a0001c0003t0001g0006 a0001c0004t0001g0025 a0001c0009t0001g0001 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32+3899C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965073 | |||||||
chr19:10965284 | A | T | 2 | a0001c0011t0001g0277 a0001c0011t0001g0278 |
2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-32+4110A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965284 | |||||||
chr19:10965306 | GC | G | 7 | a0001c0006t0001g0267 a0001c0006t0001g0270 a0001c0006t0001g0271 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32+4133delC | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965306 | |||||||
chr19:10965511 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32+4337C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965511 | |||||||
chr19:10965516 | A | G | 10 | a0001c0003t0001g0006 a0001c0004t0001g0025 a0001c0009t0001g0001 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32+4342A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965516 | |||||||
chr19:10965722 | G | C | 1 | a0001c0004t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32+4548G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965722 | |||||||
chr19:10965738 | C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+4564C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965738 | |||||||
chr19:10965823 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0171 |
2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-32+4649T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10965823 | |||||||
chr19:10965970 | G | GT | 39 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0142 others(36): Show |
39 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.-32+4825dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10965970 | ||||||
chr19:10965970 | G | GTT | 6 | a0001c0001t0001g0024 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG01081.hp2 HG01175.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+4824_-32+4825d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10965970 | ||||||
chr19:10965970 | GT | G | 91 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
91 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-32+4825delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10965970 | ||||||
chr19:10965970 | GTT | G | 8 | a0001c0001t0001g0168 a0001c0002t0001g0208 a0001c0003t0001g0209 others(5): Show |
8 | HG01168.hp2 HG01516.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32+4824_-32+4825d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10965970 | ||||||
chr19:10966323 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-32+5149G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966323 | |||||||
chr19:10966355 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-32+5181C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966355 | |||||||
chr19:10966403 | C | A | 1 | a0001c0001t0004g0282 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-32+5229C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966403 | |||||||
chr19:10966403 | C | T | 2 | a0001c0002t0001g0172 a0001c0002t0001g0174 |
2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-32+5229C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966403 | |||||||
chr19:10966557 | C | T | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32+5383C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966557 | |||||||
chr19:10966652 | G | A | 1 | a0001c0004t0001g0079 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-32+5478G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966652 | |||||||
chr19:10966670 | G | A | 90 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(87): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.-32+5496G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966670 | |||||||
chr19:10966761 | G | A | 2 | a0001c0002t0001g0238 a0001c0003t0001g0237 |
2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-32+5587G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966761 | |||||||
chr19:10966771 | C | T | 12 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(9): Show |
12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+5597C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966771 | |||||||
chr19:10966986 | G | A | 12 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(9): Show |
12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+5812G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10966986 | |||||||
chr19:10967459 | C | T | 74 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-32+6285C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967459 | |||||||
chr19:10967471 | C | T | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-32+6297C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967471 | |||||||
chr19:10967546 | G | A | 1 | a0001c0003t0001g0211 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-32+6372G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967546 | |||||||
chr19:10967685 | G | GT | 108 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0075 others(105): Show |
108 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-32+6528dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10967685 | ||||||
chr19:10967685 | G | GTT | 6 | a0001c0001t0001g0193 a0001c0002t0001g0236 a0001c0002t0001g0274 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+6527_-32+6528d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10967685 | ||||||
chr19:10967858 | A | AT | 12 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(9): Show |
12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+6693dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10967858 | ||||||
chr19:10967867 | T | A | 1 | a0001c0030t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-32+6693T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967867 | |||||||
chr19:10967894 | T | C | 1 | a0001c0011t0001g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-32+6720T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967894 | |||||||
chr19:10967916 | G | A | 1 | a0001c0004t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32+6742G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10967916 | |||||||
chr19:10968052 | C | T | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+6878C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968052 | |||||||
chr19:10968053 | A | G | 12 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(9): Show |
12 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+6879A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968053 | |||||||
chr19:10968071 | T | A | 4 | a0001c0002t0001g0213 a0001c0002t0001g0240 a0001c0002t0001g0274 others(1): Show |
4 | HG02040.hp2 HG02074.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32+6897T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968071 | |||||||
chr19:10968150 | C | T | 1 | a0001c0017t0001g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-32+6976C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968150 | |||||||
chr19:10968255 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-32+7081T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968255 | |||||||
chr19:10968379 | A | G | 2 | a0001c0001t0001g0136 a0001c0003t0001g0137 |
2 | HG01255.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-32+7205A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968379 | |||||||
chr19:10968456 | G | A | 2 | a0001c0001t0001g0166 a0001c0002t0001g0080 |
2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-32+7282G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968456 | |||||||
chr19:10968536 | C | T | 5 | a0001c0002t0001g0257 a0001c0003t0001g0206 a0001c0014t0001g0233 others(2): Show |
5 | HG00639.hp2 HG01261.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+7362C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968536 | |||||||
chr19:10968622 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-32+7448A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968622 | |||||||
chr19:10968677 | A | G | 2 | a0001c0002t0001g0172 a0001c0002t0001g0174 |
2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-32+7503A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968677 | |||||||
chr19:10968785 | C | T | 3 | a0001c0003t0001g0006 a0001c0028t0001g0007 a0001c0031t0001g0008 |
3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-32+7611C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968785 | |||||||
chr19:10968896 | G | T | 3 | a0001c0003t0001g0006 a0001c0028t0001g0007 a0001c0031t0001g0008 |
3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-32+7722G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10968896 | |||||||
chr19:10969006 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-32+7832G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969006 | |||||||
chr19:10969054 | C | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+7880C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969054 | |||||||
chr19:10969153 | A | C | 1 | a0001c0022t0001g0201 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-32+7979A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969153 | |||||||
chr19:10969176 | G | T | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-32+8002G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969176 | |||||||
chr19:10969453 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-32+8279A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969453 | |||||||
chr19:10969558 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-32+8384G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969558 | |||||||
chr19:10969589 | C | T | 1 | a0001c0022t0001g0201 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-32+8415C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969589 | |||||||
chr19:10969762 | C | T | 1 | a0001c0003t0001g0258 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-32+8588C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10969762 | |||||||
chr19:10969845 | CATT | C | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+8674_-32+8676d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10969845 | ||||||
chr19:10970089 | T | G | 3 | a0001c0002t0001g0238 a0001c0003t0001g0237 a0001c0003t0001g0241 |
3 | HG03239.hp2 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-32+8915T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970089 | |||||||
chr19:10970245 | C | T | 92 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(89): Show |
92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-32+9071C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970245 | |||||||
chr19:10970320 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-32+9146C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970320 | |||||||
chr19:10970338 | A | G | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-32+9164A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970338 | |||||||
chr19:10970407 | G | A | 6 | a0001c0001t0001g0186 a0001c0004t0001g0082 a0001c0004t0001g0083 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+9233G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970407 | |||||||
chr19:10970729 | T | C | 87 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(84): Show |
87 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.-32+9555T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970729 | |||||||
chr19:10970925 | A | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-32+9751A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970925 | |||||||
chr19:10970926 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-32+9752C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10970926 | |||||||
chr19:10971069 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-32+9895G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971069 | |||||||
chr19:10971070 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-32+9896C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971070 | |||||||
chr19:10971076 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+9902A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971076 | |||||||
chr19:10971150 | C | T | 5 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0010t0001g0009 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+9976C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971150 | |||||||
chr19:10971333 | A | G | 85 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(82): Show |
85 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-32+10159A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971333 | |||||||
chr19:10971400 | T | C | 20 | a0001c0001t0001g0024 a0001c0003t0001g0006 a0001c0007t0001g0017 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32+10226T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971400 | |||||||
chr19:10971457 | T | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0001t0001g0084 others(9): Show |
12 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+10283T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971457 | |||||||
chr19:10971490 | CT | C | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+10332delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971490 | ||||||
chr19:10971506 | T | C | 1 | a0001c0006t0001g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-32+10332T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971506 | |||||||
chr19:10971506 | TC | T | 72 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(69): Show |
72 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-32+10333delC | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971506 | |||||||
chr19:10971507 | C | T | 18 | a0001c0001t0001g0275 a0001c0002t0001g0207 a0001c0002t0001g0263 others(15): Show |
18 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-32+10333C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971507 | |||||||
chr19:10971745 | G | A | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-32+10571G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971745 | |||||||
chr19:10971748 | G | A | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+10574G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971748 | |||||||
chr19:10971761 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-32+10587C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971761 | |||||||
chr19:10971774 | C | CT | 161 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(158): Show |
161 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.-32+10617dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971774 | ||||||
chr19:10971795 | G | A | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+10621G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971795 | |||||||
chr19:10971796 | G | T | 2 | a0001c0001t0001g0037 a0001c0004t0001g0128 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-32+10622G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971796 | |||||||
chr19:10971875 | C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+10701C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971875 | |||||||
chr19:10971913 | T | C | 1 | a0001c0003t0001g0237 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-32+10739T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10971913 | |||||||
chr19:10971955 | A | AT | 6 | a0001c0001t0001g0130 a0001c0001t0001g0162 a0001c0001t0001g0265 others(3): Show |
6 | HG02074.hp1 HG02809.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+10799dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971955 | ||||||
chr19:10971955 | A | ATT | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+10798_-32+1079 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971955 | ||||||
chr19:10971955 | AT | A | 8 | a0001c0001t0001g0032 a0001c0005t0001g0242 a0001c0005t0001g0243 others(5): Show |
8 | HG00597.hp2 HG01515.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32+10799delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10971955 | ||||||
chr19:10972111 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0189 |
2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-32+10937C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972111 | |||||||
chr19:10972120 | G | A | 2 | a0001c0001t0001g0088 a0001c0002t0001g0146 |
2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.-32+10946G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972120 | |||||||
chr19:10972266 | T | C | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+11092T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972266 | |||||||
chr19:10972403 | C | CT | 71 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(68): Show |
71 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-32+11243dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10972403 | ||||||
chr19:10972534 | G | T | 75 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(72): Show |
75 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-32+11360G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972534 | |||||||
chr19:10972559 | T | C | 1 | a0001c0003t0001g0215 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-32+11385T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972559 | |||||||
chr19:10972595 | G | C | 2 | a0001c0002t0001g0207 a0001c0003t0001g0203 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-32+11421G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972595 | |||||||
chr19:10972707 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-31-11414G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972707 | |||||||
chr19:10972865 | C | T | 22 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(19): Show |
22 | HG01081.hp1 HG01167.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31-11256C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972865 | |||||||
chr19:10972895 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-31-11226G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972895 | |||||||
chr19:10972974 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-31-11147C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10972974 | |||||||
chr19:10973109 | C | CA | 24 | a0001c0001t0001g0141 a0001c0001t0001g0193 a0001c0001t0001g0194 others(21): Show |
24 | HG01081.hp1 HG01167.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-31-10997dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10973109 | ||||||
chr19:10973359 | G | T | 1 | a0001c0002t0001g0236 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-31-10762G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10973359 | |||||||
chr19:10973401 | G | T | 1 | a0001c0004t0001g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-31-10720G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10973401 | |||||||
chr19:10973407 | C | CT | 10 | a0001c0001t0004g0282 a0001c0003t0001g0006 a0001c0009t0001g0001 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31-10701dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10973407 | ||||||
chr19:10973567 | A | AT | 32 | a0001c0001t0001g0024 a0001c0001t0001g0066 a0001c0001t0001g0073 others(29): Show |
32 | HG00639.hp2 HG01081.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-31-10534dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10973567 | ||||||
chr19:10973821 | T | C | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-10300T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10973821 | |||||||
chr19:10973865 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31-10256C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10973865 | |||||||
chr19:10974033 | T | A | 2 | a0001c0002t0001g0045 a0001c0002t0001g0070 |
2 | NA18980.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-31-10088T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974033 | |||||||
chr19:10974228 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0161 |
3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-31-9893A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974228 | |||||||
chr19:10974318 | A | G | 78 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(75): Show |
78 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-31-9803A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974318 | |||||||
chr19:10974454 | CT | C | 7 | a0001c0001t0001g0162 a0001c0003t0001g0006 a0001c0004t0001g0140 others(4): Show |
7 | HG02559.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-9654delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974454 | ||||||
chr19:10974616 | C | T | 2 | a0001c0004t0001g0121 a0001c0004t0001g0160 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-31-9505C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974616 | |||||||
chr19:10974617 | G | A | 10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
10 | HG00408.hp1 HG02080.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31-9504G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974617 | |||||||
chr19:10974666 | C | CAT | 27 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0049 others(24): Show |
27 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31-9432_-31-9431d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974666 | ||||||
chr19:10974666 | C | CATAT | 8 | a0001c0001t0001g0073 a0001c0001t0001g0283 a0001c0002t0001g0034 others(5): Show |
8 | HG02145.hp2 HG03139.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31-9434_-31-9431d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974666 | ||||||
chr19:10974666 | C | CATATAT | 6 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0033 others(3): Show |
6 | HG01109.hp2 HG02976.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-9436_-31-9431d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974666 | ||||||
chr19:10974667 | A | G | 2 | a0001c0002t0001g0238 a0001c0003t0001g0237 |
2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-31-9454A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974667 | |||||||
chr19:10974681 | ATATATAT others(3): Show |
A | 1 | a0001c0006t0001g0270 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-31-9438_-31-9429d others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974681 | ||||||
chr19:10974681 | ATATATAT others(4): Show |
A | 2 | a0001c0006t0001g0271 a0001c0006t0001g0272 |
2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-31-9438_-31-9428d others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974681 | ||||||
chr19:10974683 | ATATATAT others(9): Show |
A | 2 | a0001c0007t0001g0018 a0001c0007t0001g0021 |
2 | HG02071.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-31-9436_-31-9421d others(18): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974683 | ||||||
chr19:10974685 | ATATATTT others(9): Show |
A | 8 | a0001c0007t0001g0017 a0001c0007t0001g0019 a0001c0012t0001g0013 others(5): Show |
8 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31-9434_-31-9419d others(18): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974685 | ||||||
chr19:10974685 | ATATATTT others(10): Show |
A | 1 | a0001c0001t0001g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-31-9434_-31-9418d others(19): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974685 | ||||||
chr19:10974688 | TA | T | 8 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0135 others(5): Show |
8 | HG01358.hp2 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31-9432delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974688 | |||||||
chr19:10974689 | A | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0126 a0001c0001t0001g0155 |
3 | HG01243.hp1 HG03471.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-31-9432A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974689 | |||||||
chr19:10974689 | AT | A | 65 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0042 others(62): Show |
65 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31-9397delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974689 | ||||||
chr19:10974689 | ATT | A | 38 | a0001c0001t0001g0036 a0001c0001t0001g0076 a0001c0001t0001g0085 others(35): Show |
38 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.-31-9398_-31-9397d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974689 | ||||||
chr19:10974689 | ATTT | A | 14 | a0001c0001t0001g0101 a0001c0001t0001g0193 a0001c0001t0001g0196 others(11): Show |
14 | HG01081.hp1 HG01099.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31-9399_-31-9397d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974689 | ||||||
chr19:10974689 | ATTTT | A | 9 | a0001c0001t0001g0063 a0001c0002t0001g0232 a0001c0005t0001g0242 others(6): Show |
9 | HG01884.hp2 HG01928.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31-9400_-31-9397d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10974689 | ||||||
chr19:10974690 | T | TA | 22 | a0001c0001t0001g0041 a0001c0001t0001g0058 a0001c0001t0001g0062 others(19): Show |
22 | HG00099.hp1 HG00408.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-9431_-31-9430i others(3): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974690 | |||||||
chr19:10974690 | T | TATA | 12 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0066 others(9): Show |
12 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-31-9431_-31-9430i others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974690 | |||||||
chr19:10974690 | T | TATATATA others(4): Show |
2 | a0001c0009t0001g0001 a0001c0009t0001g0002 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-9431_-31-9430i others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974690 | |||||||
chr19:10974690 | T | TATATATA others(6): Show |
1 | a0001c0009t0001g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-31-9431_-31-9430i others(15): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974690 | |||||||
chr19:10974691 | T | A | 73 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(70): Show |
73 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.-31-9430T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974691 | |||||||
chr19:10974692 | T | A | 76 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0043 others(73): Show |
76 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-31-9429T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974692 | |||||||
chr19:10974693 | T | A | 89 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(86): Show |
89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-31-9428T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974693 | |||||||
chr19:10974694 | T | A | 56 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(53): Show |
56 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-31-9427T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974694 | |||||||
chr19:10974695 | T | A | 59 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(56): Show |
59 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-31-9426T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974695 | |||||||
chr19:10974696 | T | A | 16 | a0001c0001t0001g0058 a0001c0001t0001g0100 a0001c0001t0001g0122 others(13): Show |
16 | HG01074.hp1 HG01168.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31-9425T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974696 | |||||||
chr19:10974697 | T | A | 15 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(12): Show |
15 | HG00639.hp1 HG01928.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31-9424T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974697 | |||||||
chr19:10974698 | T | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0284 a0001c0001t0001g0286 others(1): Show |
4 | HG02738.hp1 NA18979.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31-9423T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974698 | |||||||
chr19:10974699 | T | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0067 |
3 | HG01928.hp2 NA18747.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-31-9422T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974699 | |||||||
chr19:10974700 | T | A | 2 | a0001c0001t0001g0284 a0001c0025t0001g0040 |
2 | NA18979.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-31-9421T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974700 | |||||||
chr19:10974701 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-31-9420T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974701 | |||||||
chr19:10974784 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-31-9337G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974784 | |||||||
chr19:10974867 | T | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0193 a0001c0001t0001g0194 others(112): Show |
115 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-31-9254T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974867 | |||||||
chr19:10974914 | C | T | 94 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(91): Show |
94 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-31-9207C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974914 | |||||||
chr19:10974925 | C | T | 1 | a0001c0003t0001g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-31-9196C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974925 | |||||||
chr19:10974986 | C | A | 1 | a0001c0004t0001g0079 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-31-9135C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10974986 | |||||||
chr19:10975000 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-31-9121A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975000 | |||||||
chr19:10975017 | C | CT | 12 | a0001c0001t0001g0029 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
12 | HG01175.hp1 HG01192.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-31-9082dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10975017 | ||||||
chr19:10975017 | CT | C | 25 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0085 others(22): Show |
25 | HG00558.hp2 HG01071.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-31-9082delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10975017 | ||||||
chr19:10975079 | G | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-9042G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975079 | |||||||
chr19:10975318 | C | CT | 26 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(23): Show |
26 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.-31-8785dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10975318 | ||||||
chr19:10975318 | CT | C | 11 | a0001c0001t0001g0068 a0001c0001t0001g0085 a0001c0001t0001g0104 others(8): Show |
11 | HG00099.hp1 HG01515.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31-8785delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10975318 | ||||||
chr19:10975542 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-31-8579C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975542 | |||||||
chr19:10975897 | G | A | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-31-8224G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975897 | |||||||
chr19:10975913 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-31-8208A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10975913 | |||||||
chr19:10976070 | T | C | 9 | a0001c0003t0001g0006 a0001c0009t0001g0001 a0001c0009t0001g0002 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-8051T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976070 | |||||||
chr19:10976097 | C | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-8024C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976097 | |||||||
chr19:10976576 | C | T | 5 | a0001c0002t0001g0254 a0001c0002t0001g0261 a0001c0006t0001g0270 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-7545C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976576 | |||||||
chr19:10976577 | G | A | 2 | a0001c0001t0001g0029 a0001c0005t0001g0078 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-31-7544G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976577 | |||||||
chr19:10976619 | T | C | 2 | a0001c0016t0001g0228 a0001c0016t0001g0230 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-31-7502T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976619 | |||||||
chr19:10976630 | G | A | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-7491G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976630 | |||||||
chr19:10976673 | C | T | 2 | a0001c0018t0001g0039 a0001c0018t0001g0157 |
2 | NA18940.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-31-7448C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976673 | |||||||
chr19:10976710 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-31-7411C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976710 | |||||||
chr19:10976753 | C | CAA | 124 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(121): Show |
124 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-31-7353_-31-7352d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10976753 | ||||||
chr19:10976753 | C | CAAA | 47 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0044 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-31-7354_-31-7352d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10976753 | ||||||
chr19:10976770 | T | G | 172 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(169): Show |
172 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-31-7351T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976770 | |||||||
chr19:10976852 | T | C | 20 | a0001c0001t0001g0024 a0001c0003t0001g0006 a0001c0007t0001g0017 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31-7269T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976852 | |||||||
chr19:10976866 | G | A | 1 | a0001c0004t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-31-7255G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976866 | |||||||
chr19:10976920 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-31-7201G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976920 | |||||||
chr19:10976971 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-31-7150C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10976971 | |||||||
chr19:10977120 | T | C | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-31-7001T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977120 | |||||||
chr19:10977123 | C | A | 9 | a0001c0003t0001g0006 a0001c0009t0001g0001 a0001c0009t0001g0002 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-6998C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977123 | |||||||
chr19:10977214 | G | A | 7 | a0001c0006t0001g0267 a0001c0006t0001g0270 a0001c0006t0001g0271 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-6907G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977214 | |||||||
chr19:10977252 | T | C | 1 | a0001c0002t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-31-6869T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977252 | |||||||
chr19:10977543 | T | C | 170 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(167): Show |
170 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-31-6578T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977543 | |||||||
chr19:10977631 | C | A | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-6490C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977631 | |||||||
chr19:10977797 | C | T | 3 | a0001c0003t0001g0006 a0001c0028t0001g0007 a0001c0031t0001g0008 |
3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-31-6324C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977797 | |||||||
chr19:10977830 | G | T | 3 | a0001c0003t0001g0006 a0001c0028t0001g0007 a0001c0031t0001g0008 |
3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-31-6291G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10977830 | |||||||
chr19:10978042 | C | G | 5 | a0001c0001t0001g0275 a0001c0011t0001g0276 a0001c0011t0001g0277 others(2): Show |
5 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-6079C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978042 | |||||||
chr19:10978048 | C | T | 3 | a0001c0007t0001g0019 a0002c0013t0001g0016 a0002c0013t0001g0020 |
3 | HG01255.hp1 HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-31-6073C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978048 | |||||||
chr19:10978187 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0170 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-31-5934C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978187 | |||||||
chr19:10978622 | G | A | 1 | a0001c0010t0001g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-31-5499G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978622 | |||||||
chr19:10978780 | A | AAT | 3 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0133 |
3 | HG01071.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-31-5324_-31-5323d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10978780 | ||||||
chr19:10978782 | T | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0194 a0001c0001t0001g0196 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-5339T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978782 | |||||||
chr19:10978784 | T | A | 2 | a0001c0001t0001g0194 a0001c0010t0001g0011 |
2 | HG01358.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-31-5337T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978784 | |||||||
chr19:10978963 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-31-5158A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10978963 | |||||||
chr19:10979009 | G | A | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-31-5112G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979009 | |||||||
chr19:10979079 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-31-5042A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979079 | |||||||
chr19:10979119 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31-5002G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979119 | |||||||
chr19:10979125 | T | C | 2 | a0001c0018t0001g0039 a0001c0018t0001g0157 |
2 | NA18940.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-31-4996T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979125 | |||||||
chr19:10979170 | G | A | 54 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(51): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31-4951G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979170 | |||||||
chr19:10979343 | A | G | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-31-4778A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979343 | |||||||
chr19:10979412 | C | CT | 12 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0283 others(9): Show |
12 | HG01071.hp2 HG01358.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-31-4693dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10979412 | ||||||
chr19:10979412 | CT | C | 7 | a0001c0001t0001g0059 a0001c0001t0001g0076 a0001c0001t0001g0148 others(4): Show |
7 | HG01069.hp2 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31-4693delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10979412 | ||||||
chr19:10979463 | GCTCACTG others(29): Show |
G | 2 | a0001c0008t0001g0268 a0001c0008t0001g0269 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-31-4654_-31-4619d others(38): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10979463 | ||||||
chr19:10979533 | T | A | 2 | a0001c0004t0001g0167 a0003c0023t0001g0004 |
2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-4588T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979533 | |||||||
chr19:10979678 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG01167.hp2 HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-31-4443A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979678 | |||||||
chr19:10979968 | C | T | 1 | a0001c0002t0001g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-31-4153C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10979968 | |||||||
chr19:10980036 | A | G | 9 | a0001c0003t0001g0006 a0001c0009t0001g0001 a0001c0009t0001g0002 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-4085A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980036 | |||||||
chr19:10980072 | A | G | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-31-4049A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980072 | |||||||
chr19:10980165 | C | T | 9 | a0001c0003t0001g0006 a0001c0009t0001g0001 a0001c0009t0001g0002 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-3956C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980165 | |||||||
chr19:10980223 | T | C | 7 | a0001c0006t0001g0267 a0001c0006t0001g0270 a0001c0006t0001g0271 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-3898T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980223 | |||||||
chr19:10980558 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-31-3563C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980558 | |||||||
chr19:10980633 | CA | C | 276 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(273): Show |
276 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.-31-3475delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10980633 | ||||||
chr19:10980733 | G | T | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-3388G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10980733 | |||||||
chr19:10981032 | G | A | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-31-3089G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981032 | |||||||
chr19:10981052 | G | C | 1 | a0001c0016t0001g0230 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-31-3069G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981052 | |||||||
chr19:10981400 | C | G | 3 | a0001c0006t0001g0270 a0001c0006t0001g0271 a0001c0006t0001g0272 |
3 | HG02809.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31-2721C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981400 | |||||||
chr19:10981463 | G | A | 9 | a0001c0003t0001g0006 a0001c0009t0001g0001 a0001c0009t0001g0002 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-2658G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981463 | |||||||
chr19:10981585 | C | G | 2 | a0001c0016t0001g0228 a0001c0016t0001g0230 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-31-2536C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981585 | |||||||
chr19:10981711 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-31-2410C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981711 | |||||||
chr19:10981988 | C | G | 11 | a0001c0001t0001g0024 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01081.hp2 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-2133C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10981988 | |||||||
chr19:10982028 | G | A | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-31-2093G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982028 | |||||||
chr19:10982066 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-31-2055C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982066 | |||||||
chr19:10982175 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-31-1946A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982175 | |||||||
chr19:10982502 | C | CT | 18 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0052 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31-1604dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10982502 | ||||||
chr19:10982502 | CT | C | 7 | a0001c0002t0001g0254 a0001c0002t0001g0261 a0001c0009t0001g0001 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-1604delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10982502 | ||||||
chr19:10982530 | T | C | 7 | a0001c0003t0001g0260 a0001c0009t0001g0001 a0001c0009t0001g0002 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31-1591T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982530 | |||||||
chr19:10982555 | G | A | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-31-1566G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982555 | |||||||
chr19:10982568 | C | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-1553C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982568 | |||||||
chr19:10982583 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-31-1538G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982583 | |||||||
chr19:10982656 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31-1465T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982656 | |||||||
chr19:10982692 | G | A | 75 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(72): Show |
75 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-31-1429G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10982692 | |||||||
chr19:10983103 | A | G | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-31-1018A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983103 | |||||||
chr19:10983145 | A | T | 2 | a0001c0002t0001g0218 a0001c0003t0001g0222 |
2 | NA18939.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-31-976A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983145 | |||||||
chr19:10983200 | T | C | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-921T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983200 | |||||||
chr19:10983395 | T | G | 2 | a0001c0002t0001g0207 a0001c0003t0001g0203 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-31-726T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983395 | |||||||
chr19:10983433 | G | GT | 9 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0002t0001g0274 others(6): Show |
9 | HG01109.hp1 HG01175.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-671dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr19 | 10983433 | ||||||
chr19:10983503 | G | A | 2 | a0001c0004t0001g0167 a0003c0023t0001g0004 |
2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-618G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983503 | |||||||
chr19:10983537 | C | T | 1 | a0001c0018t0001g0157 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-31-584C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983537 | |||||||
chr19:10983818 | C | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-303C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983818 | |||||||
chr19:10983900 | G | A | 1 | a0001c0005t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-31-221G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983900 | |||||||
chr19:10983915 | C | T | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-206C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10983915 | |||||||
chr19:10984107 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31-14G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 1/34 | chr19 | 10984107 | |||||||
chr19:10984492 | T | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0152 |
2 | HG01884.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.222+119T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10984492 | |||||||
chr19:10984804 | C | G | 1 | a0001c0001t0001g0046 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.222+431C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10984804 | |||||||
chr19:10985034 | T | C | 19 | a0001c0003t0001g0006 a0001c0007t0001g0017 a0001c0007t0001g0018 others(16): Show |
19 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.223-239T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985034 | |||||||
chr19:10985096 | C | T | 2 | a0001c0004t0001g0071 a0001c0004t0001g0185 |
2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.223-177C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985096 | |||||||
chr19:10985154 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.223-119G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985154 | |||||||
chr19:10985155 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.223-118C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985155 | |||||||
chr19:10985181 | G | A | 1 | a0001c0004t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.223-92G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985181 | |||||||
chr19:10985220 | T | C | 19 | a0001c0003t0001g0006 a0001c0007t0001g0017 a0001c0007t0001g0018 others(16): Show |
19 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.223-53T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985220 | |||||||
chr19:10985231 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0171 |
2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.223-42G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 2/34 | chr19 | 10985231 | |||||||
chr19:10985700 | C | G | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+295C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/34 | chr19 | 10985700 | |||||||
chr19:10985934 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.356-255C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/34 | chr19 | 10985934 | |||||||
chr19:10986151 | T | C | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.356-38T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/34 | chr19 | 10986151 | |||||||
chr19:10986175 | A | G | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.356-14A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 3/34 | chr19 | 10986175 | |||||||
chr19:10986667 | C | T | 2 | a0001c0002t0001g0218 a0001c0003t0001g0222 |
2 | NA18939.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.760+74C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/34 | chr19 | 10986667 | |||||||
chr19:10986709 | G | A | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.760+116G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/34 | chr19 | 10986709 | |||||||
chr19:10986774 | C | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.761-131C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/34 | chr19 | 10986774 | |||||||
chr19:10986869 | C | T | 2 | a0001c0008t0001g0268 a0001c0008t0001g0269 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.761-36C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 4/34 | chr19 | 10986869 | |||||||
chr19:10987033 | C | T | 4 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+30C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987033 | |||||||
chr19:10987034 | G | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.859+31G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987034 | |||||||
chr19:10987094 | G | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.859+91G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987094 | |||||||
chr19:10987096 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.859+93C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987096 | |||||||
chr19:10987131 | T | C | 3 | a0001c0007t0001g0019 a0002c0013t0001g0016 a0002c0013t0001g0020 |
3 | HG01255.hp1 HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.859+128T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987131 | |||||||
chr19:10987146 | C | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.859+143C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987146 | |||||||
chr19:10987178 | G | A | 2 | a0001c0002t0001g0080 a0001c0002t0001g0239 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.859+175G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987178 | |||||||
chr19:10987475 | C | T | 1 | a0001c0032t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.860-191C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987475 | |||||||
chr19:10987633 | A | G | 1 | a0001c0027t0001g0014 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.860-33A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 5/34 | chr19 | 10987633 | |||||||
chr19:10988124 | CT | C | 10 | a0001c0001t0001g0064 a0001c0001t0001g0129 a0001c0008t0001g0266 others(7): Show |
10 | HG02698.hp1 HG02738.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1118+213delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chr19 | 10988124 | ||||||
chr19:10988607 | G | T | 2 | a0001c0002t0001g0207 a0001c0003t0001g0203 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1118+683G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10988607 | |||||||
chr19:10988780 | C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1119-537C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10988780 | |||||||
chr19:10988933 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1119-384C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10988933 | |||||||
chr19:10989040 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1119-277C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989040 | |||||||
chr19:10989047 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1119-270C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989047 | |||||||
chr19:10989089 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1119-228C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989089 | |||||||
chr19:10989099 | A | G | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1119-218A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989099 | |||||||
chr19:10989303 | G | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1119-14G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 6/34 | chr19 | 10989303 | |||||||
chr19:10989702 | T | TC | 7 | a0001c0007t0001g0018 a0001c0007t0001g0019 a0001c0007t0001g0021 others(4): Show |
7 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245+262dupC | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr19 | 10989702 | ||||||
chr19:10989705 | C | CT | 103 | a0001c0001t0001g0050 a0001c0001t0001g0099 a0001c0001t0001g0100 others(100): Show |
103 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1245+277dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr19 | 10989705 | ||||||
chr19:10989705 | CT | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0052 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1245+277delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr19 | 10989705 | ||||||
chr19:10989706 | T | C | 3 | a0001c0007t0001g0017 a0001c0012t0001g0013 a0001c0012t0001g0015 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1245+263T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10989706 | |||||||
chr19:10989726 | C | CA | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | NA18941.hp1 NA18942.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245+284dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr19 | 10989726 | ||||||
chr19:10989784 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1245+341C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10989784 | |||||||
chr19:10989785 | A | G | 16 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.1245+342A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10989785 | |||||||
chr19:10989952 | C | T | 4 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1245+509C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10989952 | |||||||
chr19:10990000 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1245+557G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990000 | |||||||
chr19:10990058 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1245+615C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990058 | |||||||
chr19:10990097 | C | T | 1 | a0001c0007t0001g0018 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1245+654C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990097 | |||||||
chr19:10990312 | C | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1246-838C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990312 | |||||||
chr19:10990329 | A | C | 7 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0103 others(4): Show |
7 | NA18747.hp1 NA18948.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.1246-821A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990329 | |||||||
chr19:10990435 | G | A | 1 | a0001c0003t0001g0217 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1246-715G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990435 | |||||||
chr19:10990553 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1246-597C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990553 | |||||||
chr19:10990633 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1246-517G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990633 | |||||||
chr19:10990633 | G | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1246-517G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990633 | |||||||
chr19:10990757 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1246-393C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990757 | |||||||
chr19:10990883 | C | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1246-267C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990883 | |||||||
chr19:10990943 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1246-207A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10990943 | |||||||
chr19:10991007 | G | A | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-143G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10991007 | |||||||
chr19:10991084 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1246-66C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10991084 | |||||||
chr19:10991124 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1246-26C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 7/34 | chr19 | 10991124 | |||||||
chr19:10991331 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0152 |
2 | HG01884.hp1 HG01952.hp1 |
splice_region_variant&intron_variant | LOW | c.1419+8C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991331 | |||||||
chr19:10991466 | T | C | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1419+143T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991466 | |||||||
chr19:10991496 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1419+173T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991496 | |||||||
chr19:10991543 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1419+220G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991543 | |||||||
chr19:10991920 | G | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0126 others(1): Show |
4 | HG01975.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1419+597G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10991920 | |||||||
chr19:10992086 | G | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1419+763G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992086 | |||||||
chr19:10992391 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1419+1068G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992391 | |||||||
chr19:10992420 | A | AT | 27 | a0001c0001t0001g0044 a0001c0001t0001g0122 a0001c0001t0001g0126 others(24): Show |
27 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1419+1118dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10992420 | ||||||
chr19:10992420 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1419+1097A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992420 | |||||||
chr19:10992420 | AT | A | 6 | a0001c0001t0001g0116 a0001c0001t0004g0282 a0001c0010t0001g0009 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1419+1118delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10992420 | ||||||
chr19:10992456 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1419+1133C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992456 | |||||||
chr19:10992573 | C | T | 1 | a0001c0002t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1419+1250C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992573 | |||||||
chr19:10992784 | T | C | 2 | a0001c0025t0001g0040 a0001c0026t0001g0281 |
2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1419+1461T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992784 | |||||||
chr19:10992834 | G | A | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1419+1511G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992834 | |||||||
chr19:10992878 | A | G | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1419+1555A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992878 | |||||||
chr19:10992942 | A | G | 1 | a0001c0020t0001g0234 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1419+1619A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10992942 | |||||||
chr19:10992984 | C | CT | 6 | a0001c0001t0001g0145 a0001c0002t0001g0208 a0001c0002t0001g0263 others(3): Show |
6 | HG01192.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1419+1680dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10992984 | ||||||
chr19:10992984 | CT | C | 11 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0001g0126 others(8): Show |
11 | HG01975.hp1 HG02040.hp2 HG03490.hp2 others(8): Show |
intron_variant | MODIFIER | c.1419+1680delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10992984 | ||||||
chr19:10993081 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1420-1747G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993081 | |||||||
chr19:10993132 | T | G | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1420-1696T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993132 | |||||||
chr19:10993337 | T | C | 1 | a0001c0004t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1420-1491T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993337 | |||||||
chr19:10993445 | C | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420-1383C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993445 | |||||||
chr19:10993560 | C | T | 5 | a0001c0005t0001g0078 a0001c0005t0001g0242 a0001c0005t0001g0243 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420-1268C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993560 | |||||||
chr19:10993690 | C | G | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420-1138C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10993690 | |||||||
chr19:10994071 | A | G | 107 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(104): Show |
107 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1420-757A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994071 | |||||||
chr19:10994215 | G | A | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420-613G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994215 | |||||||
chr19:10994318 | G | GT | 52 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0038 others(49): Show |
52 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1420-487dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10994318 | ||||||
chr19:10994318 | GT | G | 6 | a0001c0001t0001g0176 a0001c0001t0001g0283 a0001c0002t0001g0208 others(3): Show |
6 | HG02698.hp2 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-487delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr19 | 10994318 | ||||||
chr19:10994328 | T | G | 31 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0046 others(28): Show |
31 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1420-500T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994328 | |||||||
chr19:10994346 | C | G | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1420-482C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994346 | |||||||
chr19:10994468 | C | T | 2 | a0001c0008t0001g0268 a0001c0008t0001g0269 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1420-360C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994468 | |||||||
chr19:10994543 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1420-285C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994543 | |||||||
chr19:10994710 | CT | C | 6 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 others(3): Show |
6 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-117delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 8/34 | chr19 | 10994710 | |||||||
chr19:10995189 | C | G | 7 | a0001c0006t0001g0267 a0001c0006t0001g0270 a0001c0006t0001g0271 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1593+188C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995189 | |||||||
chr19:10995216 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1593+215C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995216 | |||||||
chr19:10995243 | G | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1593+242G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995243 | |||||||
chr19:10995376 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1593+375C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995376 | |||||||
chr19:10995626 | T | C | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1594-587T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995626 | |||||||
chr19:10995672 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1594-541G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995672 | |||||||
chr19:10995924 | C | T | 103 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(100): Show |
103 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1594-289C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10995924 | |||||||
chr19:10996078 | C | T | 3 | a0001c0006t0001g0270 a0001c0006t0001g0271 a0001c0006t0001g0272 |
3 | HG02809.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1594-135C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10996078 | |||||||
chr19:10996114 | T | C | 113 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(110): Show |
113 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1594-99T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 9/34 | chr19 | 10996114 | |||||||
chr19:10996409 | G | A | 5 | a0001c0002t0001g0207 a0001c0003t0001g0203 a0001c0010t0001g0009 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+29G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 10/34 | chr19 | 10996409 | |||||||
chr19:10996457 | T | C | 111 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(108): Show |
111 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1762-37T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 10/34 | chr19 | 10996457 | |||||||
chr19:10996458 | G | A | 7 | a0001c0006t0001g0267 a0001c0006t0001g0270 a0001c0006t0001g0271 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-36G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 10/34 | chr19 | 10996458 | |||||||
chr19:10996619 | G | A | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1812+75G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10996619 | |||||||
chr19:10996920 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(5): Show |
8 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1812+376T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10996920 | |||||||
chr19:10996994 | T | G | 4 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1812+450T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10996994 | |||||||
chr19:10996996 | C | T | 1 | a0001c0032t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1812+452C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10996996 | |||||||
chr19:10997093 | C | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1812+549C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997093 | |||||||
chr19:10997111 | G | A | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1812+567G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997111 | |||||||
chr19:10997159 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1812+615A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997159 | |||||||
chr19:10997433 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1812+889C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997433 | |||||||
chr19:10997447 | TC | T | 35 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0046 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1812+906delC | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 10997447 | ||||||
chr19:10997518 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1812+974G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997518 | |||||||
chr19:10997617 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1812+1073C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997617 | |||||||
chr19:10997620 | C | T | 1 | a0001c0015t0001g0023 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1812+1076C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997620 | |||||||
chr19:10997693 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1812+1149C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997693 | |||||||
chr19:10997847 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1812+1303A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997847 | |||||||
chr19:10997891 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1812+1347C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10997891 | |||||||
chr19:10998062 | T | G | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1812+1518T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998062 | |||||||
chr19:10998328 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1812+1784C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998328 | |||||||
chr19:10998329 | G | A | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1812+1785G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998329 | |||||||
chr19:10998503 | C | CTTT | 13 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(10): Show |
13 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1812+1972_1812+197 others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 10998503 | ||||||
chr19:10998521 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1812+1977C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998521 | |||||||
chr19:10998792 | A | G | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1812+2248A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998792 | |||||||
chr19:10998839 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1812+2295T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998839 | |||||||
chr19:10998948 | C | T | 2 | a0001c0001t0001g0166 a0001c0003t0001g0006 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1812+2404C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10998948 | |||||||
chr19:10999022 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1812+2478C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999022 | |||||||
chr19:10999046 | G | C | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1812+2502G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999046 | |||||||
chr19:10999308 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1812+2764G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999308 | |||||||
chr19:10999414 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1812+2870T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999414 | |||||||
chr19:10999993 | A | G | 2 | a0001c0025t0001g0040 a0001c0026t0001g0281 |
2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1813-3036A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 10999993 | |||||||
chr19:11000048 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1813-2981A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000048 | |||||||
chr19:11000227 | CA | C | 17 | a0001c0001t0001g0097 a0001c0002t0001g0232 a0001c0002t0001g0239 others(14): Show |
17 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1813-2787delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11000227 | ||||||
chr19:11000407 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1813-2622A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000407 | |||||||
chr19:11000676 | C | A | 1 | a0001c0001t0001g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1813-2353C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000676 | |||||||
chr19:11000739 | C | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1813-2290C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000739 | |||||||
chr19:11000803 | G | A | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1813-2226G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000803 | |||||||
chr19:11000841 | C | CA | 92 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(89): Show |
92 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1813-2187dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11000841 | ||||||
chr19:11000859 | C | CA | 17 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0057 others(14): Show |
17 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.1813-2153dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11000859 | ||||||
chr19:11000878 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1813-2151T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11000878 | |||||||
chr19:11001167 | A | G | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1813-1862A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001167 | |||||||
chr19:11001475 | C | T | 109 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(106): Show |
109 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1813-1554C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001475 | |||||||
chr19:11001477 | T | A | 109 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(106): Show |
109 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1813-1552T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001477 | |||||||
chr19:11001658 | C | G | 17 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(14): Show |
17 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1813-1371C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001658 | |||||||
chr19:11001659 | T | TGACCCTC | 17 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(14): Show |
17 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1813-1370_1813-136 others(11): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001659 | |||||||
chr19:11001758 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0004t0001g0128 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1813-1271G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001758 | |||||||
chr19:11001765 | T | C | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1813-1264T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001765 | |||||||
chr19:11001814 | C | T | 6 | a0001c0001t0001g0186 a0001c0004t0001g0082 a0001c0004t0001g0083 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1813-1215C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11001814 | |||||||
chr19:11002007 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0153 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1813-1022A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002007 | |||||||
chr19:11002280 | C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1813-749C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002280 | |||||||
chr19:11002281 | T | C | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1813-748T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002281 | |||||||
chr19:11002346 | A | C | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1813-683A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002346 | |||||||
chr19:11002351 | C | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1813-678C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002351 | |||||||
chr19:11002389 | G | C | 1 | a0001c0017t0001g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1813-640G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002389 | |||||||
chr19:11002401 | C | T | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | NA18941.hp1 NA18942.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.1813-628C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002401 | |||||||
chr19:11002431 | A | G | 11 | a0001c0002t0001g0080 a0001c0002t0001g0232 a0001c0002t0001g0239 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1813-598A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002431 | |||||||
chr19:11002503 | A | AAAAT | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1813-522_1813-519d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11002503 | ||||||
chr19:11002507 | TA | T | 6 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1813-517delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11002507 | ||||||
chr19:11002534 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1813-495C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002534 | |||||||
chr19:11002605 | C | T | 4 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1813-424C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002605 | |||||||
chr19:11002799 | CA | C | 81 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0093 others(78): Show |
81 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1813-208delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11002799 | ||||||
chr19:11002799 | CAA | C | 28 | a0001c0002t0001g0208 a0001c0002t0001g0232 a0001c0003t0001g0006 others(25): Show |
28 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1813-209_1813-208d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr19 | 11002799 | ||||||
chr19:11002819 | A | G | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1813-210A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002819 | |||||||
chr19:11002821 | A | G | 2 | a0001c0016t0001g0228 a0001c0016t0001g0230 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1813-208A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002821 | |||||||
chr19:11002844 | G | A | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1813-185G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002844 | |||||||
chr19:11002975 | T | C | 20 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1813-54T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 11/34 | chr19 | 11002975 | |||||||
chr19:11003226 | G | A | 73 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(70): Show |
73 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1943+67G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 12/34 | chr19 | 11003226 | |||||||
chr19:11003321 | G | T | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1944-19G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 12/34 | chr19 | 11003321 | |||||||
chr19:11003328 | C | T | 4 | a0001c0002t0001g0218 a0001c0003t0001g0217 a0001c0003t0001g0222 others(1): Show |
4 | NA18939.hp2 NA18940.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944-12C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 12/34 | chr19 | 11003328 | |||||||
chr19:11003530 | C | T | 68 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(65): Show |
68 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.2001+133C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003530 | |||||||
chr19:11003531 | G | T | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2001+134G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003531 | |||||||
chr19:11003537 | G | A | 2 | a0001c0002t0001g0223 a0001c0002t0001g0229 |
2 | NA18947.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2001+140G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003537 | |||||||
chr19:11003676 | A | G | 12 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0001t0001g0084 others(9): Show |
12 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.2001+279A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003676 | |||||||
chr19:11003711 | A | AT | 13 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0133 others(10): Show |
13 | HG01928.hp2 HG01981.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2001+332dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11003711 | ||||||
chr19:11003711 | A | T | 11 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(8): Show |
11 | HG01081.hp1 HG01167.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001+314A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003711 | |||||||
chr19:11003799 | C | A | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2001+402C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003799 | |||||||
chr19:11003815 | A | C | 2 | a0001c0016t0001g0228 a0001c0016t0001g0230 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2001+418A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003815 | |||||||
chr19:11003915 | T | C | 89 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(86): Show |
89 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2001+518T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11003915 | |||||||
chr19:11004004 | G | A | 2 | a0001c0002t0001g0207 a0001c0003t0001g0203 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2001+607G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004004 | |||||||
chr19:11004112 | G | A | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2001+715G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004112 | |||||||
chr19:11004173 | T | C | 2 | a0001c0002t0001g0247 a0001c0002t0001g0251 |
2 | HG02135.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2001+776T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004173 | |||||||
chr19:11004248 | T | C | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2001+851T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004248 | |||||||
chr19:11004253 | AT | A | 99 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(96): Show |
99 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2001+870delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11004253 | ||||||
chr19:11004253 | ATT | A | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2001+869_2001+870d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11004253 | ||||||
chr19:11004402 | C | T | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2001+1005C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004402 | |||||||
chr19:11004431 | A | G | 4 | a0001c0002t0001g0232 a0001c0002t0001g0273 a0001c0030t0001g0212 others(1): Show |
4 | HG02083.hp1 HG03490.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001+1034A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004431 | |||||||
chr19:11004634 | A | G | 1 | a0001c0002t0001g0261 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2001+1237A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004634 | |||||||
chr19:11004811 | G | GT | 20 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2001+1422dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11004811 | ||||||
chr19:11004845 | CT | C | 99 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(96): Show |
99 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2001+1460delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11004845 | ||||||
chr19:11004870 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0154 |
2 | HG00597.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2001+1473C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004870 | |||||||
chr19:11004920 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2001+1523A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004920 | |||||||
chr19:11004935 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0059 a0001c0001t0001g0265 others(1): Show |
4 | HG00639.hp1 NA18954.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001+1538G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11004935 | |||||||
chr19:11005116 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2001+1719G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005116 | |||||||
chr19:11005331 | T | C | 1 | a0001c0002t0001g0232 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2001+1934T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005331 | |||||||
chr19:11005419 | G | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2001+2022G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005419 | |||||||
chr19:11005483 | G | A | 20 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2001+2086G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005483 | |||||||
chr19:11005590 | C | T | 14 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0101 others(11): Show |
14 | HG01099.hp1 HG01109.hp1 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.2001+2193C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005590 | |||||||
chr19:11005619 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2001+2222T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005619 | |||||||
chr19:11005929 | A | G | 7 | a0001c0006t0001g0267 a0001c0006t0001g0270 a0001c0006t0001g0271 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002-1973A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11005929 | |||||||
chr19:11006232 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2002-1670G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006232 | |||||||
chr19:11006276 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2002-1626C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006276 | |||||||
chr19:11006554 | C | T | 2 | a0001c0002t0001g0207 a0001c0003t0001g0203 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2002-1348C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006554 | |||||||
chr19:11006570 | A | G | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2002-1332A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006570 | |||||||
chr19:11006581 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2002-1321T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006581 | |||||||
chr19:11006760 | T | C | 20 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2002-1142T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006760 | |||||||
chr19:11006895 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0086 |
2 | HG01167.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2002-1007G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006895 | |||||||
chr19:11006949 | T | C | 1 | a0001c0017t0001g0031 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2002-953T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006949 | |||||||
chr19:11006951 | A | G | 20 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2002-951A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006951 | |||||||
chr19:11006979 | C | T | 14 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2002-923C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11006979 | |||||||
chr19:11007140 | C | T | 2 | a0001c0002t0001g0247 a0001c0002t0001g0251 |
2 | HG02135.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2002-762C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007140 | |||||||
chr19:11007298 | C | T | 2 | a0001c0012t0001g0013 a0001c0012t0001g0015 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2002-604C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007298 | |||||||
chr19:11007375 | C | T | 1 | a0001c0003t0001g0244 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2002-527C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007375 | |||||||
chr19:11007416 | T | C | 3 | a0001c0002t0001g0238 a0001c0003t0001g0237 a0001c0003t0001g0241 |
3 | HG03239.hp2 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2002-486T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007416 | |||||||
chr19:11007429 | C | CA | 17 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0119 others(14): Show |
17 | HG00558.hp1 HG00621.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2002-450dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11007429 | ||||||
chr19:11007429 | CA | C | 22 | a0001c0001t0001g0029 a0001c0001t0001g0064 a0001c0001t0001g0067 others(19): Show |
22 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.2002-450delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11007429 | ||||||
chr19:11007429 | CAAAAAAA | C | 7 | a0001c0006t0001g0267 a0001c0006t0001g0270 a0001c0006t0001g0271 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002-456_2002-450d others(9): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr19 | 11007429 | ||||||
chr19:11007808 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2002-94A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007808 | |||||||
chr19:11007883 | T | C | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2002-19T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 13/34 | chr19 | 11007883 | |||||||
chr19:11008035 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2123+12C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008035 | |||||||
chr19:11008085 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+62T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008085 | |||||||
chr19:11008086 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+63G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008086 | |||||||
chr19:11008087 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+64G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008087 | |||||||
chr19:11008093 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+70A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008093 | |||||||
chr19:11008094 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+71T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008094 | |||||||
chr19:11008095 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+72C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008095 | |||||||
chr19:11008097 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+74C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008097 | |||||||
chr19:11008098 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2123+75A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008098 | |||||||
chr19:11008120 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0170 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2123+97G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008120 | |||||||
chr19:11008214 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2123+191C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008214 | |||||||
chr19:11008518 | G | A | 2 | a0001c0012t0001g0013 a0001c0012t0001g0015 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2123+495G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008518 | |||||||
chr19:11008540 | G | A | 7 | a0001c0001t0001g0182 a0001c0009t0001g0001 a0001c0009t0001g0002 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.2123+517G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008540 | |||||||
chr19:11008596 | G | C | 158 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(155): Show |
158 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.2123+573G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008596 | |||||||
chr19:11008616 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2123+593C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008616 | |||||||
chr19:11008641 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2123+618C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008641 | |||||||
chr19:11008659 | G | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2123+636G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008659 | |||||||
chr19:11008973 | C | CA | 14 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0161 others(11): Show |
14 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2123+964dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11008973 | ||||||
chr19:11008975 | A | C | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2123+952A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11008975 | |||||||
chr19:11009007 | C | CT | 13 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
13 | HG00408.hp2 HG02109.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.2123+1018dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | C | CTT | 23 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0033 others(20): Show |
23 | HG00438.hp2 HG00673.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.2123+1017_2123+101 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | C | CTTT | 27 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0036 others(24): Show |
27 | HG00597.hp1 HG00639.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.2123+1016_2123+101 others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | C | CTTTT | 33 | a0001c0001t0001g0032 a0001c0001t0001g0073 a0001c0001t0001g0100 others(30): Show |
33 | HG00597.hp2 HG00621.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.2123+1015_2123+101 others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | C | CTTTTT | 18 | a0001c0001t0001g0059 a0001c0001t0001g0096 a0001c0001t0001g0103 others(15): Show |
18 | HG01952.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2123+1014_2123+101 others(9): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | C | CTTTTTT | 6 | a0001c0001t0001g0037 a0001c0001t0001g0118 a0001c0001t0001g0162 others(3): Show |
6 | HG02717.hp1 HG02897.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2123+1013_2123+101 others(10): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | C | CTTTTTTT others(11): Show |
1 | a0001c0010t0001g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2123+1001_2123+101 others(22): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CT | C | 16 | a0001c0001t0001g0024 a0001c0001t0001g0084 a0001c0001t0001g0090 others(13): Show |
16 | HG00438.hp1 HG00735.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2123+1018delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CTT | C | 29 | a0001c0001t0001g0041 a0001c0001t0001g0077 a0001c0001t0001g0081 others(26): Show |
29 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.2123+1017_2123+101 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CTTTTTTT others(1): Show |
C | 22 | a0001c0002t0001g0061 a0001c0002t0001g0070 a0001c0002t0001g0072 others(19): Show |
22 | HG00544.hp2 HG01099.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.2123+1011_2123+101 others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CTTTTTTT others(2): Show |
C | 64 | a0001c0001t0001g0200 a0001c0002t0001g0034 a0001c0002t0001g0045 others(61): Show |
64 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2123+1010_2123+101 others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CTTTTTTT others(3): Show |
C | 5 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0007t0001g0017 others(2): Show |
5 | HG02735.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2123+1009_2123+101 others(14): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2123+1008_2123+101 others(15): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0047 a0001c0026t0001g0281 |
3 | NA18906.hp1 NA19005.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2123+1006_2123+101 others(17): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0161 |
3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2123+1005_2123+101 others(18): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009007 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2123+1001_2123+101 others(22): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009007 | ||||||
chr19:11009120 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2123+1097C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009120 | |||||||
chr19:11009138 | C | T | 1 | a0001c0003t0001g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2123+1115C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009138 | |||||||
chr19:11009278 | C | T | 3 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0163 |
3 | HG02258.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2124-1103C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009278 | |||||||
chr19:11009354 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2124-1027G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009354 | |||||||
chr19:11009612 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0161 |
3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2124-769C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009612 | |||||||
chr19:11009687 | C | CT | 15 | a0001c0001t0001g0058 a0001c0001t0001g0142 a0001c0001t0001g0283 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.2124-675dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr19 | 11009687 | ||||||
chr19:11009877 | C | T | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2124-504C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009877 | |||||||
chr19:11009934 | A | C | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2124-447A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009934 | |||||||
chr19:11009938 | C | T | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2124-443C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11009938 | |||||||
chr19:11010007 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2124-374G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11010007 | |||||||
chr19:11010261 | C | T | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2124-120C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11010261 | |||||||
chr19:11010323 | G | A | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2124-58G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 14/34 | chr19 | 11010323 | |||||||
chr19:11010649 | A | G | 1 | a0001c0003t0001g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2274+118A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11010649 | |||||||
chr19:11010735 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2274+204C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11010735 | |||||||
chr19:11011003 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2274+472G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011003 | |||||||
chr19:11011193 | G | A | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2274+662G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011193 | |||||||
chr19:11011287 | C | A | 7 | a0001c0006t0001g0267 a0001c0006t0001g0270 a0001c0006t0001g0271 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2274+756C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011287 | |||||||
chr19:11011343 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2274+812G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011343 | |||||||
chr19:11011394 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2274+863T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011394 | |||||||
chr19:11011718 | G | T | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2274+1187G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011718 | |||||||
chr19:11011776 | C | G | 2 | a0001c0004t0001g0071 a0001c0004t0001g0185 |
2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2275-1173C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011776 | |||||||
chr19:11011824 | T | A | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2275-1125T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011824 | |||||||
chr19:11011855 | G | T | 11 | a0001c0002t0001g0080 a0001c0002t0001g0232 a0001c0002t0001g0239 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.2275-1094G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011855 | |||||||
chr19:11011932 | C | G | 4 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2275-1017C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11011932 | |||||||
chr19:11012034 | G | T | 8 | a0001c0002t0001g0245 a0001c0002t0001g0250 a0001c0003t0001g0211 others(5): Show |
8 | HG00099.hp1 HG01074.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2275-915G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012034 | |||||||
chr19:11012264 | T | G | 1 | a0001c0011t0001g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2275-685T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012264 | |||||||
chr19:11012415 | T | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0133 |
3 | HG01071.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2275-534T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012415 | |||||||
chr19:11012522 | C | G | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2275-427C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012522 | |||||||
chr19:11012722 | G | A | 1 | a0001c0011t0001g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2275-227G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012722 | |||||||
chr19:11012736 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2275-213C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012736 | |||||||
chr19:11012760 | C | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2275-189C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012760 | |||||||
chr19:11012911 | G | A | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2275-38G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012911 | |||||||
chr19:11012946 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.2275-3C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 15/34 | chr19 | 11012946 | |||||||
chr19:11013155 | G | A | 1 | a0001c0007t0001g0017 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2438+43G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013155 | |||||||
chr19:11013161 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2438+49G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013161 | |||||||
chr19:11013419 | C | G | 15 | a0001c0002t0001g0080 a0001c0002t0001g0146 a0001c0002t0001g0232 others(12): Show |
15 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2438+307C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013419 | |||||||
chr19:11013794 | C | G | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2438+682C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013794 | |||||||
chr19:11013976 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2438+864A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013976 | |||||||
chr19:11013976 | A | T | 1 | a0001c0004t0001g0128 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2438+864A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11013976 | |||||||
chr19:11014292 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2438+1180A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014292 | |||||||
chr19:11014308 | G | A | 1 | a0001c0005t0001g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2438+1196G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014308 | |||||||
chr19:11014511 | C | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2438+1399C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014511 | |||||||
chr19:11014540 | C | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0176 a0001c0027t0001g0014 |
3 | HG01099.hp1 HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2438+1428C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014540 | |||||||
chr19:11014782 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2438+1670A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014782 | |||||||
chr19:11014821 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0179 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2438+1709T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014821 | |||||||
chr19:11014931 | G | A | 5 | a0001c0001t0001g0186 a0001c0004t0001g0082 a0001c0004t0001g0083 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2438+1819G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014931 | |||||||
chr19:11014961 | C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2438+1849C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11014961 | |||||||
chr19:11015124 | A | G | 3 | a0001c0003t0001g0006 a0001c0028t0001g0007 a0001c0031t0001g0008 |
3 | HG02922.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2438+2012A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015124 | |||||||
chr19:11015237 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2438+2125G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015237 | |||||||
chr19:11015284 | T | C | 113 | a0001c0001t0001g0205 a0001c0002t0001g0034 a0001c0002t0001g0045 others(110): Show |
113 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.2438+2172T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015284 | |||||||
chr19:11015484 | T | C | 8 | a0001c0002t0001g0245 a0001c0002t0001g0250 a0001c0003t0001g0211 others(5): Show |
8 | HG00099.hp1 HG01074.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2438+2372T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015484 | |||||||
chr19:11015521 | T | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0133 |
3 | HG01071.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2438+2409T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015521 | |||||||
chr19:11015523 | G | C | 75 | a0001c0001t0001g0205 a0001c0002t0001g0034 a0001c0002t0001g0045 others(72): Show |
75 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2438+2411G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015523 | |||||||
chr19:11015589 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2438+2477C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015589 | |||||||
chr19:11015597 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2438+2485C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015597 | |||||||
chr19:11015604 | C | T | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2438+2492C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015604 | |||||||
chr19:11015967 | T | C | 112 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(109): Show |
112 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.2438+2855T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11015967 | |||||||
chr19:11016007 | T | G | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2438+2895T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016007 | |||||||
chr19:11016393 | G | T | 75 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(72): Show |
75 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.2439-2564G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016393 | |||||||
chr19:11016422 | T | C | 1 | a0001c0002t0001g0261 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2439-2535T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016422 | |||||||
chr19:11016530 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2439-2427G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016530 | |||||||
chr19:11016551 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2439-2406G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016551 | |||||||
chr19:11016700 | T | C | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2439-2257T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016700 | |||||||
chr19:11016729 | T | A | 1 | a0001c0003t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2439-2228T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016729 | |||||||
chr19:11016981 | C | T | 2 | a0001c0002t0001g0273 a0001c0032t0001g0231 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2439-1976C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11016981 | |||||||
chr19:11017047 | C | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2439-1910C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017047 | |||||||
chr19:11017096 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0058 others(1): Show |
4 | HG00408.hp2 NA19009.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439-1861C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017096 | |||||||
chr19:11017136 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2439-1821C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017136 | |||||||
chr19:11017243 | G | A | 3 | a0001c0002t0001g0207 a0001c0003t0001g0203 a0001c0024t0001g0012 |
3 | HG02145.hp2 HG03453.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2439-1714G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017243 | |||||||
chr19:11017257 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2439-1700G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017257 | |||||||
chr19:11017332 | C | G | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2439-1625C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017332 | |||||||
chr19:11017387 | G | A | 8 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2439-1570G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017387 | |||||||
chr19:11017686 | G | T | 1 | a0001c0017t0001g0031 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2439-1271G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017686 | |||||||
chr19:11017689 | C | T | 1 | a0001c0003t0001g0137 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2439-1268C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017689 | |||||||
chr19:11017874 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2439-1083G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017874 | |||||||
chr19:11017920 | A | G | 157 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(154): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.2439-1037A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11017920 | |||||||
chr19:11018148 | T | C | 113 | a0001c0001t0001g0205 a0001c0002t0001g0034 a0001c0002t0001g0045 others(110): Show |
113 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.2439-809T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018148 | |||||||
chr19:11018217 | C | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0187 |
2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2439-740C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018217 | |||||||
chr19:11018264 | G | A | 1 | a0001c0003t0001g0149 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2439-693G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018264 | |||||||
chr19:11018293 | C | T | 13 | a0001c0002t0001g0080 a0001c0002t0001g0232 a0001c0002t0001g0239 others(10): Show |
13 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.2439-664C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018293 | |||||||
chr19:11018425 | G | A | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0282 others(1): Show |
4 | NA18947.hp1 NA18957.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439-532G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018425 | |||||||
chr19:11018492 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2439-465C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018492 | |||||||
chr19:11018604 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2439-353G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018604 | |||||||
chr19:11018663 | T | C | 8 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2439-294T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018663 | |||||||
chr19:11018753 | C | G | 237 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(234): Show |
237 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.2439-204C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018753 | |||||||
chr19:11018845 | C | T | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2439-112C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018845 | |||||||
chr19:11018924 | C | T | 10 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0101 others(7): Show |
10 | HG01099.hp1 HG03669.hp2 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.2439-33C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 16/34 | chr19 | 11018924 | |||||||
chr19:11019129 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2505+106C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 17/34 | chr19 | 11019129 | |||||||
chr19:11019204 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2505+181C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 17/34 | chr19 | 11019204 | |||||||
chr19:11019438 | G | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2506-153G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 17/34 | chr19 | 11019438 | |||||||
chr19:11019519 | G | A | 22 | a0001c0002t0001g0080 a0001c0002t0001g0207 a0001c0002t0001g0232 others(19): Show |
22 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.2506-72G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 17/34 | chr19 | 11019519 | |||||||
chr19:11019755 | G | A | 2 | a0001c0001t0001g0026 a0001c0024t0001g0012 |
2 | HG01109.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2616+54G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11019755 | |||||||
chr19:11019759 | C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2616+58C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11019759 | |||||||
chr19:11019766 | C | T | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616+65C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11019766 | |||||||
chr19:11019833 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2616+132C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11019833 | |||||||
chr19:11020057 | A | T | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2616+356A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020057 | |||||||
chr19:11020415 | G | GT | 8 | a0001c0001t0001g0065 a0001c0001t0001g0154 a0001c0001t0001g0194 others(5): Show |
8 | HG00597.hp1 NA18953.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.2616+727dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr19 | 11020415 | ||||||
chr19:11020513 | C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2616+812C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020513 | |||||||
chr19:11020546 | G | T | 4 | a0001c0002t0001g0208 a0001c0011t0001g0276 a0001c0011t0001g0277 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2616+845G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020546 | |||||||
chr19:11020564 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0265 |
2 | NA18954.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2616+863C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020564 | |||||||
chr19:11020599 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2616+898T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020599 | |||||||
chr19:11020674 | C | T | 2 | a0001c0006t0001g0270 a0001c0006t0001g0272 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2616+973C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020674 | |||||||
chr19:11020727 | T | C | 8 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2617-998T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11020727 | |||||||
chr19:11021260 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2617-465G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021260 | |||||||
chr19:11021404 | G | A | 74 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(71): Show |
74 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2617-321G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021404 | |||||||
chr19:11021504 | G | T | 2 | a0001c0006t0001g0270 a0001c0006t0001g0272 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2617-221G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021504 | |||||||
chr19:11021639 | G | A | 28 | a0001c0002t0001g0080 a0001c0002t0001g0146 a0001c0002t0001g0207 others(25): Show |
28 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.2617-86G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021639 | |||||||
chr19:11021721 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG00621.hp1 | splice_region_variant&intron_variant | LOW | c.2617-4G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 18/34 | chr19 | 11021721 | |||||||
chr19:11022049 | C | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2859+82C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022049 | |||||||
chr19:11022249 | A | C | 30 | a0001c0002t0001g0080 a0001c0002t0001g0146 a0001c0002t0001g0207 others(27): Show |
30 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.2859+282A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022249 | |||||||
chr19:11022380 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2859+413G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022380 | |||||||
chr19:11022596 | A | G | 112 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(109): Show |
112 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.2859+629A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022596 | |||||||
chr19:11022643 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2859+676C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022643 | |||||||
chr19:11022655 | C | T | 1 | a0001c0005t0001g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2859+688C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11022655 | |||||||
chr19:11023017 | C | T | 2 | a0001c0002t0001g0238 a0001c0003t0001g0237 |
2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2860-501C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023017 | |||||||
chr19:11023043 | A | G | 31 | a0001c0001t0001g0158 a0001c0002t0001g0080 a0001c0002t0001g0146 others(28): Show |
31 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.2860-475A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023043 | |||||||
chr19:11023151 | C | T | 14 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0001t0001g0084 others(11): Show |
14 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.2860-367C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023151 | |||||||
chr19:11023282 | C | T | 3 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 |
3 | HG02698.hp1 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2860-236C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023282 | |||||||
chr19:11023414 | A | G | 65 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(62): Show |
65 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.2860-104A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 19/34 | chr19 | 11023414 | |||||||
chr19:11023752 | G | C | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2973+121G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11023752 | |||||||
chr19:11024011 | A | G | 1 | a0001c0004t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2974-320A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024011 | |||||||
chr19:11024018 | T | C | 75 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(72): Show |
75 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2974-313T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024018 | |||||||
chr19:11024024 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0126 a0001c0001t0001g0153 |
3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2974-307C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024024 | |||||||
chr19:11024076 | G | A | 5 | a0001c0002t0001g0257 a0001c0003t0001g0206 a0001c0014t0001g0233 others(2): Show |
5 | HG00639.hp2 HG01261.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2974-255G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024076 | |||||||
chr19:11024102 | G | C | 1 | a0001c0010t0001g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2974-229G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 20/34 | chr19 | 11024102 | |||||||
chr19:11024612 | A | C | 1 | a0001c0003t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3081+174A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024612 | |||||||
chr19:11024613 | G | C | 1 | a0001c0003t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3081+175G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024613 | |||||||
chr19:11024649 | G | T | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3081+211G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024649 | |||||||
chr19:11024978 | T | C | 155 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(152): Show |
155 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.3082-444T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024978 | |||||||
chr19:11024992 | C | G | 1 | a0001c0001t0001g0283 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3082-430C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024992 | |||||||
chr19:11024993 | G | C | 1 | a0001c0001t0001g0283 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3082-429G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11024993 | |||||||
chr19:11025339 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3082-83C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 21/34 | chr19 | 11025339 | |||||||
chr19:11025539 | C | G | 158 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(155): Show |
158 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.3168+31C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025539 | |||||||
chr19:11025566 | G | A | 1 | a0001c0003t0001g0227 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3168+58G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025566 | |||||||
chr19:11025628 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0155 |
2 | HG01243.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3168+120T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025628 | |||||||
chr19:11025639 | C | T | 150 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(147): Show |
150 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.3168+131C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025639 | |||||||
chr19:11025663 | A | G | 1 | a0001c0011t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3168+155A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025663 | |||||||
chr19:11025671 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0073 |
3 | HG00597.hp2 NA18995.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3168+163C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025671 | |||||||
chr19:11025776 | T | G | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3168+268T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025776 | |||||||
chr19:11025777 | C | T | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3168+269C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025777 | |||||||
chr19:11025833 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3168+325C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025833 | |||||||
chr19:11025939 | T | G | 2 | a0001c0011t0001g0277 a0001c0011t0001g0278 |
2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3169-361T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11025939 | |||||||
chr19:11026106 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3169-194G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11026106 | |||||||
chr19:11026181 | C | T | 64 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(61): Show |
64 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.3169-119C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11026181 | |||||||
chr19:11026183 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3169-117T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11026183 | |||||||
chr19:11026184 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3169-116G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 22/34 | chr19 | 11026184 | |||||||
chr19:11026459 | T | C | 11 | a0001c0004t0001g0005 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.3215+113T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026459 | |||||||
chr19:11026497 | C | CT | 65 | a0001c0001t0001g0084 a0001c0001t0001g0102 a0001c0001t0001g0104 others(62): Show |
65 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.3215+170dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr19 | 11026497 | ||||||
chr19:11026497 | CT | C | 57 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(54): Show |
57 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.3215+170delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr19 | 11026497 | ||||||
chr19:11026666 | T | G | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3215+320T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026666 | |||||||
chr19:11026753 | C | G | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+407C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026753 | |||||||
chr19:11026755 | T | C | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+409T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026755 | |||||||
chr19:11026756 | C | T | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+410C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026756 | |||||||
chr19:11026777 | G | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3215+431G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026777 | |||||||
chr19:11026788 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3215+442C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026788 | |||||||
chr19:11026794 | C | T | 2 | a0001c0025t0001g0040 a0001c0026t0001g0281 |
2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3215+448C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026794 | |||||||
chr19:11026810 | A | G | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3215+464A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026810 | |||||||
chr19:11026898 | C | T | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+552C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026898 | |||||||
chr19:11026899 | T | C | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3215+553T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11026899 | |||||||
chr19:11027491 | G | C | 155 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(152): Show |
155 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.3216-293G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11027491 | |||||||
chr19:11027550 | T | C | 63 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(60): Show |
63 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3216-234T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11027550 | |||||||
chr19:11027616 | A | G | 11 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
11 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3216-168A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 23/34 | chr19 | 11027616 | |||||||
chr19:11028055 | C | T | 1 | a0001c0003t0001g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3382+105C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028055 | |||||||
chr19:11028199 | G | C | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3382+249G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028199 | |||||||
chr19:11028406 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3382+456C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028406 | |||||||
chr19:11028632 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3382+682C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028632 | |||||||
chr19:11028665 | G | A | 1 | a0001c0003t0001g0137 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3382+715G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028665 | |||||||
chr19:11028772 | G | C | 2 | a0001c0002t0001g0208 a0001c0028t0001g0007 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3382+822G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028772 | |||||||
chr19:11028842 | C | G | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3382+892C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028842 | |||||||
chr19:11028960 | G | T | 153 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(150): Show |
153 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.3382+1010G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028960 | |||||||
chr19:11028980 | C | G | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3382+1030C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028980 | |||||||
chr19:11028981 | T | G | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3382+1031T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11028981 | |||||||
chr19:11029057 | C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3382+1107C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029057 | |||||||
chr19:11029070 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0187 |
2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3382+1120A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029070 | |||||||
chr19:11029220 | G | A | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3382+1270G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029220 | |||||||
chr19:11029468 | A | G | 64 | a0001c0001t0001g0205 a0001c0002t0001g0034 a0001c0002t0001g0045 others(61): Show |
64 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.3383-1262A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029468 | |||||||
chr19:11029593 | G | A | 1 | a0001c0030t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3383-1137G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029593 | |||||||
chr19:11029723 | G | A | 1 | a0001c0002t0001g0034 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3383-1007G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029723 | |||||||
chr19:11029755 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0161 |
3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3383-975C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029755 | |||||||
chr19:11029818 | C | T | 1 | a0001c0020t0001g0234 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3383-912C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029818 | |||||||
chr19:11029917 | C | T | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3383-813C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029917 | |||||||
chr19:11029972 | G | A | 2 | a0001c0003t0001g0006 a0001c0031t0001g0008 |
2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3383-758G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029972 | |||||||
chr19:11029991 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0156 a0001c0001t0001g0164 |
3 | HG00621.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3383-739C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11029991 | |||||||
chr19:11030027 | T | C | 157 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(154): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.3383-703T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030027 | |||||||
chr19:11030543 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3383-187G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030543 | |||||||
chr19:11030605 | C | T | 2 | a0001c0003t0001g0006 a0001c0031t0001g0008 |
2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3383-125C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030605 | |||||||
chr19:11030669 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3383-61G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030669 | |||||||
chr19:11030677 | C | T | 3 | a0001c0002t0001g0238 a0001c0003t0001g0237 a0001c0003t0001g0241 |
3 | HG03239.hp2 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3383-53C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 24/34 | chr19 | 11030677 | |||||||
chr19:11031070 | C | T | 1 | a0001c0003t0001g0211 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3546+177C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11031070 | |||||||
chr19:11031348 | C | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3546+455C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11031348 | |||||||
chr19:11031768 | G | C | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3546+875G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11031768 | |||||||
chr19:11031949 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3546+1056C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11031949 | |||||||
chr19:11032020 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0133 |
2 | HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3546+1127G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032020 | |||||||
chr19:11032075 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3546+1182G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032075 | |||||||
chr19:11032093 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3547-1197G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032093 | |||||||
chr19:11032119 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3547-1171C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032119 | |||||||
chr19:11032163 | C | T | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3547-1127C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032163 | |||||||
chr19:11032202 | C | T | 1 | a0001c0002t0001g0240 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3547-1088C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032202 | |||||||
chr19:11032447 | A | G | 1 | a0001c0005t0001g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3547-843A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032447 | |||||||
chr19:11032572 | A | G | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3547-718A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032572 | |||||||
chr19:11032666 | C | CA | 80 | a0001c0001t0001g0052 a0001c0001t0001g0075 a0001c0001t0001g0148 others(77): Show |
80 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.3547-609dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr19 | 11032666 | ||||||
chr19:11032666 | CA | C | 6 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG03491.hp2 NA18941.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.3547-609delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr19 | 11032666 | ||||||
chr19:11032777 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3547-513G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032777 | |||||||
chr19:11032945 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3547-345A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032945 | |||||||
chr19:11032959 | C | T | 2 | a0001c0004t0001g0121 a0001c0004t0001g0160 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3547-331C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032959 | |||||||
chr19:11032960 | G | A | 11 | a0001c0002t0001g0080 a0001c0002t0001g0232 a0001c0002t0001g0239 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.3547-330G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032960 | |||||||
chr19:11032986 | G | A | 16 | a0001c0004t0001g0005 a0001c0005t0001g0078 a0001c0005t0001g0242 others(13): Show |
16 | HG01255.hp1 HG01516.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.3547-304G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11032986 | |||||||
chr19:11033011 | C | T | 19 | a0001c0002t0001g0080 a0001c0002t0001g0207 a0001c0002t0001g0232 others(16): Show |
19 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.3547-279C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11033011 | |||||||
chr19:11033135 | C | G | 76 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(73): Show |
76 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3547-155C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11033135 | |||||||
chr19:11033279 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3547-11T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 25/34 | chr19 | 11033279 | |||||||
chr19:11033691 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3775-76G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 26/34 | chr19 | 11033691 | |||||||
chr19:11034018 | C | T | 1 | a0001c0003t0001g0249 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3874-105C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 27/34 | chr19 | 11034018 | |||||||
chr19:11034067 | G | A | 1 | a0001c0003t0001g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3874-56G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 27/34 | chr19 | 11034067 | |||||||
chr19:11034284 | G | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3951+84G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034284 | |||||||
chr19:11034411 | C | T | 1 | a0001c0004t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3951+211C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034411 | |||||||
chr19:11034449 | G | T | 1 | a0001c0001t0001g0285 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3951+249G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034449 | |||||||
chr19:11034582 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3952-332A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034582 | |||||||
chr19:11034639 | G | A | 1 | a0001c0001t0004g0282 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3952-275G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 28/34 | chr19 | 11034639 | |||||||
chr19:11035148 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4170+16G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035148 | |||||||
chr19:11035165 | G | A | 1 | a0001c0006t0001g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4170+33G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035165 | |||||||
chr19:11035177 | G | A | 11 | a0001c0001t0001g0081 a0001c0007t0001g0017 a0001c0007t0001g0018 others(8): Show |
11 | HG01071.hp1 HG01255.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.4170+45G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035177 | |||||||
chr19:11035276 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4170+144A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035276 | |||||||
chr19:11035286 | T | C | 3 | a0001c0006t0001g0270 a0001c0006t0001g0271 a0001c0006t0001g0272 |
3 | HG02809.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4170+154T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035286 | |||||||
chr19:11035390 | T | C | 2 | a0001c0001t0001g0026 a0001c0024t0001g0012 |
2 | HG01109.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4170+258T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035390 | |||||||
chr19:11035430 | T | C | 3 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 |
3 | HG02698.hp1 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.4170+298T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035430 | |||||||
chr19:11035569 | C | G | 2 | a0001c0002t0001g0208 a0001c0028t0001g0007 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4170+437C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035569 | |||||||
chr19:11035569 | C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4170+437C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035569 | |||||||
chr19:11035571 | C | A | 1 | a0001c0002t0001g0146 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4170+439C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035571 | |||||||
chr19:11035662 | T | C | 153 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(150): Show |
153 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.4170+530T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035662 | |||||||
chr19:11035823 | T | C | 215 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(212): Show |
215 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.4170+691T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11035823 | |||||||
chr19:11036108 | C | T | 1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4170+976C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036108 | |||||||
chr19:11036182 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4170+1050G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036182 | |||||||
chr19:11036379 | C | T | 1 | a0001c0001t0004g0282 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4170+1247C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036379 | |||||||
chr19:11036505 | C | T | 1 | a0001c0032t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4170+1373C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036505 | |||||||
chr19:11036534 | C | T | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4170+1402C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036534 | |||||||
chr19:11036566 | G | T | 1 | a0001c0002t0001g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4170+1434G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036566 | |||||||
chr19:11036625 | A | C | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4170+1493A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036625 | |||||||
chr19:11036653 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4170+1521C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036653 | |||||||
chr19:11036678 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0156 others(1): Show |
4 | HG00621.hp2 NA18954.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.4170+1546G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036678 | |||||||
chr19:11036850 | T | C | 1 | a0001c0027t0001g0014 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4170+1718T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036850 | |||||||
chr19:11036936 | C | T | 46 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(43): Show |
46 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.4170+1804C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036936 | |||||||
chr19:11036939 | G | A | 153 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(150): Show |
153 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.4170+1807G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11036939 | |||||||
chr19:11037018 | T | G | 158 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(155): Show |
158 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.4170+1886T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037018 | |||||||
chr19:11037120 | G | A | 1 | a0001c0005t0001g0262 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4170+1988G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037120 | |||||||
chr19:11037211 | A | G | 2 | a0001c0011t0001g0276 a0001c0021t0001g0175 |
2 | HG02698.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4170+2079A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037211 | |||||||
chr19:11037408 | A | G | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4170+2276A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037408 | |||||||
chr19:11037437 | C | G | 152 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(149): Show |
152 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.4170+2305C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037437 | |||||||
chr19:11037612 | C | T | 2 | a0001c0003t0001g0006 a0001c0031t0001g0008 |
2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4170+2480C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037612 | |||||||
chr19:11037909 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4170+2777T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11037909 | |||||||
chr19:11038009 | C | T | 1 | a0002c0013t0001g0020 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4170+2877C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038009 | |||||||
chr19:11038061 | C | T | 12 | a0001c0002t0001g0080 a0001c0002t0001g0146 a0001c0002t0001g0232 others(9): Show |
12 | HG00544.hp2 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.4170+2929C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038061 | |||||||
chr19:11038093 | A | G | 1 | a0001c0004t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4170+2961A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038093 | |||||||
chr19:11038105 | T | C | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4170+2973T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038105 | |||||||
chr19:11038147 | C | T | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4170+3015C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038147 | |||||||
chr19:11038258 | C | G | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4171-3049C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038258 | |||||||
chr19:11038272 | A | G | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4171-3035A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038272 | |||||||
chr19:11038453 | G | A | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.4171-2854G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038453 | |||||||
chr19:11038473 | T | G | 1 | a0001c0003t0001g0217 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4171-2834T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038473 | |||||||
chr19:11038555 | A | C | 3 | a0001c0002t0001g0263 a0001c0016t0001g0228 a0001c0016t0001g0230 |
3 | HG02965.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4171-2752A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038555 | |||||||
chr19:11038626 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4171-2681G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038626 | |||||||
chr19:11038698 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0179 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4171-2609G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038698 | |||||||
chr19:11038924 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4171-2383A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11038924 | |||||||
chr19:11039309 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4171-1998G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039309 | |||||||
chr19:11039325 | G | T | 3 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 |
3 | HG02698.hp1 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.4171-1982G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039325 | |||||||
chr19:11039337 | G | C | 7 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0126 others(4): Show |
7 | HG01975.hp2 HG03490.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.4171-1970G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039337 | |||||||
chr19:11039546 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4171-1761C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039546 | |||||||
chr19:11039711 | G | A | 2 | a0001c0012t0001g0013 a0001c0012t0001g0015 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4171-1596G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039711 | |||||||
chr19:11039834 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0150 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4171-1473G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039834 | |||||||
chr19:11039865 | G | A | 1 | a0001c0004t0001g0083 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4171-1442G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039865 | |||||||
chr19:11039885 | A | G | 1 | a0001c0003t0001g0149 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4171-1422A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039885 | |||||||
chr19:11039888 | C | G | 1 | a0001c0004t0001g0121 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4171-1419C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11039888 | |||||||
chr19:11040223 | C | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4171-1084C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040223 | |||||||
chr19:11040251 | G | A | 2 | a0001c0002t0001g0080 a0001c0002t0001g0239 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4171-1056G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040251 | |||||||
chr19:11040323 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4171-984G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040323 | |||||||
chr19:11040383 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0176 a0001c0027t0001g0014 |
3 | HG01099.hp1 HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4171-924A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040383 | |||||||
chr19:11040449 | A | G | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.4171-858A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040449 | |||||||
chr19:11040591 | C | CA | 10 | a0001c0001t0001g0024 a0001c0001t0001g0091 a0001c0001t0001g0107 others(7): Show |
10 | HG00099.hp2 HG01081.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.4171-697dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr19 | 11040591 | ||||||
chr19:11040591 | CA | C | 101 | a0001c0001t0001g0086 a0001c0001t0001g0135 a0001c0002t0001g0034 others(98): Show |
101 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.4171-697delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr19 | 11040591 | ||||||
chr19:11040591 | CAA | C | 45 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.4171-698_4171-697d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr19 | 11040591 | ||||||
chr19:11040654 | T | C | 151 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(148): Show |
151 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.4171-653T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040654 | |||||||
chr19:11040788 | C | T | 1 | a0001c0003t0001g0215 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4171-519C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040788 | |||||||
chr19:11040916 | C | T | 1 | a0001c0002t0001g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4171-391C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040916 | |||||||
chr19:11040977 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4171-330A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11040977 | |||||||
chr19:11041010 | C | T | 11 | a0001c0002t0001g0080 a0001c0002t0001g0232 a0001c0002t0001g0239 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.4171-297C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11041010 | |||||||
chr19:11041206 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4171-101G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11041206 | |||||||
chr19:11041216 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4171-91G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 29/34 | chr19 | 11041216 | |||||||
chr19:11041681 | C | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+121C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11041681 | |||||||
chr19:11041718 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4424+158A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11041718 | |||||||
chr19:11041974 | C | T | 44 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(41): Show |
44 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.4424+414C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11041974 | |||||||
chr19:11042119 | G | C | 11 | a0001c0002t0001g0080 a0001c0002t0001g0232 a0001c0002t0001g0239 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.4424+559G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042119 | |||||||
chr19:11042158 | A | G | 2 | a0001c0002t0001g0208 a0001c0028t0001g0007 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4424+598A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042158 | |||||||
chr19:11042162 | C | G | 1 | a0001c0015t0001g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4424+602C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042162 | |||||||
chr19:11042212 | G | A | 5 | a0001c0002t0001g0257 a0001c0003t0001g0206 a0001c0014t0001g0233 others(2): Show |
5 | HG00639.hp2 HG01261.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.4424+652G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042212 | |||||||
chr19:11042271 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4424+711C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042271 | |||||||
chr19:11042423 | G | A | 1 | a0001c0003t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4424+863G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042423 | |||||||
chr19:11042700 | C | T | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+1140C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042700 | |||||||
chr19:11042779 | G | A | 1 | a0001c0002t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4424+1219G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042779 | |||||||
chr19:11042867 | T | C | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4424+1307T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042867 | |||||||
chr19:11042898 | C | T | 10 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0019 others(7): Show |
10 | HG01255.hp1 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4424+1338C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11042898 | |||||||
chr19:11043144 | C | A | 150 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(147): Show |
150 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.4424+1584C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043144 | |||||||
chr19:11043523 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4424+1963A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043523 | |||||||
chr19:11043655 | T | TA | 8 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0048 others(5): Show |
8 | HG01069.hp2 HG01099.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.4424+2102dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11043655 | ||||||
chr19:11043674 | C | T | 3 | a0001c0010t0001g0009 a0001c0010t0001g0010 a0001c0010t0001g0011 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.4424+2114C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043674 | |||||||
chr19:11043776 | C | T | 74 | a0001c0001t0001g0190 a0001c0002t0001g0034 a0001c0002t0001g0045 others(71): Show |
74 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.4424+2216C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043776 | |||||||
chr19:11043851 | G | A | 2 | a0001c0001t0001g0026 a0001c0024t0001g0012 |
2 | HG01109.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4424+2291G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043851 | |||||||
chr19:11043983 | A | C | 2 | a0001c0016t0001g0228 a0001c0016t0001g0230 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.4424+2423A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11043983 | |||||||
chr19:11044139 | A | G | 1 | a0001c0028t0001g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4424+2579A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044139 | |||||||
chr19:11044234 | CTG | C | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+2677_4424+267 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11044234 | ||||||
chr19:11044304 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4424+2744A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044304 | |||||||
chr19:11044308 | A | G | 1 | a0001c0028t0001g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4424+2748A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044308 | |||||||
chr19:11044451 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4424+2891C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044451 | |||||||
chr19:11044608 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4424+3048C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044608 | |||||||
chr19:11044619 | G | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+3059G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044619 | |||||||
chr19:11044732 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0283 |
3 | NA18944.hp2 NA18980.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.4424+3172G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044732 | |||||||
chr19:11044796 | A | T | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4424+3236A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044796 | |||||||
chr19:11044883 | A | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0265 |
2 | NA18954.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.4424+3323A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11044883 | |||||||
chr19:11045059 | G | A | 45 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.4424+3499G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11045059 | |||||||
chr19:11045176 | C | T | 1 | a0001c0003t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4424+3616C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11045176 | |||||||
chr19:11045318 | T | TA | 8 | a0001c0001t0001g0085 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG01192.hp2 HG01515.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.4424+3769dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11045318 | ||||||
chr19:11045642 | CT | C | 7 | a0001c0001t0001g0086 a0001c0001t0001g0097 a0001c0001t0001g0104 others(4): Show |
7 | HG02896.hp1 HG02922.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.4424+4096delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11045642 | ||||||
chr19:11045668 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4424+4108C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11045668 | |||||||
chr19:11045875 | G | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+4315G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11045875 | |||||||
chr19:11046132 | A | C | 3 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 |
3 | HG02698.hp1 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.4424+4572A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046132 | |||||||
chr19:11046191 | C | T | 6 | a0001c0002t0001g0207 a0001c0009t0001g0001 a0001c0009t0001g0002 others(3): Show |
6 | HG02559.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4424+4631C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046191 | |||||||
chr19:11046209 | C | T | 1 | a0001c0002t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4424+4649C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046209 | |||||||
chr19:11046222 | C | CA | 23 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0065 others(20): Show |
23 | HG00408.hp2 HG00639.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.4424+4678dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046222 | ||||||
chr19:11046385 | G | A | 11 | a0001c0002t0001g0080 a0001c0002t0001g0232 a0001c0002t0001g0239 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.4424+4825G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046385 | |||||||
chr19:11046506 | C | T | 1 | a0001c0030t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4424+4946C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046506 | |||||||
chr19:11046592 | C | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4424+5032C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046592 | |||||||
chr19:11046681 | G | A | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4424+5121G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046681 | |||||||
chr19:11046747 | A | G | 78 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(75): Show |
78 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.4424+5187A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046747 | |||||||
chr19:11046886 | C | T | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4424+5326C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046886 | |||||||
chr19:11046948 | C | CA | 14 | a0001c0001t0001g0032 a0001c0001t0001g0093 a0001c0001t0001g0119 others(11): Show |
14 | HG00544.hp1 HG00597.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.4424+5407dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046948 | ||||||
chr19:11046948 | C | CAA | 51 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0044 others(48): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.4424+5406_4424+540 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046948 | ||||||
chr19:11046948 | C | CAAA | 17 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0058 others(14): Show |
17 | HG01255.hp1 HG01516.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.4424+5405_4424+540 others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046948 | ||||||
chr19:11046948 | CA | C | 77 | a0001c0001t0001g0028 a0001c0001t0001g0123 a0001c0001t0001g0161 others(74): Show |
77 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.4424+5407delA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11046948 | ||||||
chr19:11046983 | C | T | 2 | a0001c0002t0001g0273 a0001c0032t0001g0231 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4424+5423C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11046983 | |||||||
chr19:11047049 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4424+5489C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047049 | |||||||
chr19:11047179 | G | A | 2 | a0001c0008t0001g0268 a0001c0008t0001g0269 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4424+5619G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047179 | |||||||
chr19:11047190 | T | C | 3 | a0001c0011t0001g0277 a0001c0011t0001g0278 a0001c0032t0001g0231 |
3 | HG02738.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4424+5630T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047190 | |||||||
chr19:11047226 | A | G | 1 | a0001c0003t0001g0224 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4424+5666A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047226 | |||||||
chr19:11047243 | A | G | 29 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0086 others(26): Show |
29 | HG01255.hp2 HG01358.hp1 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.4424+5683A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047243 | |||||||
chr19:11047259 | G | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0112 a0001c0001t0001g0120 others(7): Show |
10 | HG02257.hp1 HG02970.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.4424+5699G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047259 | |||||||
chr19:11047342 | A | G | 3 | a0001c0001t0001g0166 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4424+5782A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047342 | |||||||
chr19:11047355 | T | C | 1 | a0001c0026t0001g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4424+5795T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047355 | |||||||
chr19:11047358 | C | T | 14 | a0001c0001t0001g0076 a0001c0001t0001g0168 a0001c0001t0001g0171 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.4424+5798C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047358 | |||||||
chr19:11047371 | A | T | 173 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.4424+5811A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047371 | |||||||
chr19:11047379 | C | T | 282 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(279): Show |
282 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.4424+5819C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047379 | |||||||
chr19:11047410 | G | GT | 60 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0053 others(57): Show |
60 | HG00408.hp2 HG01175.hp2 HG01255.hp1 others(57): Show |
intron_variant | MODIFIER | c.4424+5865dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047410 | ||||||
chr19:11047410 | G | GTT | 7 | a0001c0001t0001g0130 a0001c0001t0001g0142 a0001c0002t0001g0146 others(4): Show |
7 | HG00544.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4424+5864_4424+586 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047410 | ||||||
chr19:11047410 | GTT | G | 114 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(111): Show |
114 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.4424+5864_4424+586 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047410 | ||||||
chr19:11047473 | A | G | 1 | a0001c0003t0001g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4424+5913A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047473 | |||||||
chr19:11047583 | AT | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0170 a0001c0002t0001g0208 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4424+6029delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047583 | ||||||
chr19:11047656 | C | T | 1 | a0001c0011t0001g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4424+6096C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047656 | |||||||
chr19:11047657 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4424+6097G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047657 | |||||||
chr19:11047958 | T | A | 1 | a0001c0005t0001g0262 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4424+6398T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11047958 | |||||||
chr19:11047958 | TTTA | T | 3 | a0001c0001t0001g0190 a0001c0007t0001g0018 a0001c0007t0001g0021 |
3 | HG02071.hp2 HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.4424+6413_4424+641 others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11047958 | ||||||
chr19:11048046 | C | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4424+6486C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048046 | |||||||
chr19:11048230 | T | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0114 a0001c0001t0001g0118 others(1): Show |
4 | NA18971.hp2 NA19005.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.4424+6670T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048230 | |||||||
chr19:11048319 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4424+6759C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048319 | |||||||
chr19:11048400 | G | A | 69 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0052 others(66): Show |
69 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.4424+6840G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048400 | |||||||
chr19:11048409 | G | T | 2 | a0001c0003t0001g0204 a0001c0003t0001g0214 |
2 | HG02080.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.4424+6849G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048409 | |||||||
chr19:11048420 | G | T | 38 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0131 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4424+6860G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048420 | |||||||
chr19:11048554 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0120 a0001c0001t0001g0170 others(1): Show |
4 | HG02922.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4424+6994G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048554 | |||||||
chr19:11048773 | C | T | 24 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(21): Show |
24 | HG01175.hp2 HG01255.hp1 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.4424+7213C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048773 | |||||||
chr19:11048849 | G | T | 39 | a0001c0001t0001g0165 a0001c0002t0001g0247 a0001c0002t0001g0251 others(36): Show |
39 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.4424+7289G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11048849 | |||||||
chr19:11049033 | G | T | 2 | a0001c0008t0001g0268 a0001c0008t0001g0269 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4424+7473G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049033 | |||||||
chr19:11049167 | G | A | 1 | a0001c0002t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4424+7607G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049167 | |||||||
chr19:11049213 | T | C | 40 | a0001c0001t0001g0165 a0001c0002t0001g0247 a0001c0002t0001g0251 others(37): Show |
40 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.4424+7653T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049213 | |||||||
chr19:11049226 | C | T | 6 | a0001c0008t0001g0268 a0001c0008t0001g0269 a0001c0011t0001g0276 others(3): Show |
6 | HG02280.hp2 HG02698.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.4424+7666C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049226 | |||||||
chr19:11049340 | G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4424+7780G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049340 | |||||||
chr19:11049429 | G | T | 1 | a0001c0002t0001g0232 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4424+7869G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049429 | |||||||
chr19:11049485 | G | GT | 6 | a0001c0001t0001g0122 a0001c0001t0001g0142 a0001c0001t0001g0145 others(3): Show |
6 | HG01192.hp2 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4424+7942dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11049485 | ||||||
chr19:11049485 | G | T | 26 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0102 others(23): Show |
26 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.4424+7925G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049485 | |||||||
chr19:11049485 | GT | G | 44 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0002t0001g0247 others(41): Show |
44 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.4424+7942delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11049485 | ||||||
chr19:11049492 | T | G | 1 | a0001c0004t0001g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4424+7932T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049492 | |||||||
chr19:11049493 | T | G | 41 | a0001c0001t0001g0165 a0001c0002t0001g0247 a0001c0002t0001g0251 others(38): Show |
41 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.4424+7933T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049493 | |||||||
chr19:11049502 | T | G | 2 | a0001c0016t0001g0228 a0001c0031t0001g0008 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4424+7942T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049502 | |||||||
chr19:11049789 | G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4424+8229G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049789 | |||||||
chr19:11049856 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4424+8296C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049856 | |||||||
chr19:11049932 | G | A | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4425-8323G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049932 | |||||||
chr19:11049953 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0170 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4425-8302T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11049953 | |||||||
chr19:11050110 | G | C | 2 | a0001c0008t0001g0268 a0001c0008t0001g0269 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4425-8145G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050110 | |||||||
chr19:11050167 | G | A | 2 | a0001c0001t0001g0177 a0001c0002t0001g0236 |
2 | HG02040.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.4425-8088G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050167 | |||||||
chr19:11050252 | G | T | 1 | a0001c0004t0001g0083 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4425-8003G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050252 | |||||||
chr19:11050283 | C | T | 1 | a0001c0002t0001g0247 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4425-7972C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050283 | |||||||
chr19:11050708 | A | G | 1 | a0001c0002t0001g0279 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4425-7547A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050708 | |||||||
chr19:11050851 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4425-7404A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050851 | |||||||
chr19:11050861 | C | A | 38 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0131 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-7394C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050861 | |||||||
chr19:11050869 | T | C | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4425-7386T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11050869 | |||||||
chr19:11051201 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4425-7054C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051201 | |||||||
chr19:11051309 | A | G | 2 | a0001c0010t0001g0009 a0001c0010t0001g0010 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4425-6946A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051309 | |||||||
chr19:11051322 | G | A | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4425-6933G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051322 | |||||||
chr19:11051368 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4425-6887G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051368 | |||||||
chr19:11051415 | C | G | 1 | a0001c0019t0001g0192 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4425-6840C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051415 | |||||||
chr19:11051465 | G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-6790G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051465 | |||||||
chr19:11051491 | C | CT | 22 | a0001c0001t0001g0058 a0001c0001t0001g0141 a0001c0001t0001g0168 others(19): Show |
22 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.4425-6746dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11051491 | ||||||
chr19:11051491 | C | CTT | 8 | a0001c0003t0001g0203 a0001c0004t0001g0025 a0001c0004t0001g0082 others(5): Show |
8 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4425-6747_4425-674 others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11051491 | ||||||
chr19:11051491 | CT | C | 9 | a0001c0001t0001g0066 a0001c0001t0001g0097 a0001c0001t0001g0104 others(6): Show |
9 | HG01168.hp1 HG02280.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.4425-6746delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11051491 | ||||||
chr19:11051522 | C | T | 2 | a0001c0008t0001g0268 a0001c0008t0001g0269 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4425-6733C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051522 | |||||||
chr19:11051547 | G | T | 1 | a0001c0014t0001g0235 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4425-6708G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051547 | |||||||
chr19:11051615 | C | T | 4 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.4425-6640C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051615 | |||||||
chr19:11051660 | T | C | 1 | a0001c0002t0001g0273 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4425-6595T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051660 | |||||||
chr19:11051699 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0275 |
2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4425-6556T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11051699 | |||||||
chr19:11052203 | T | C | 1 | a0001c0007t0001g0021 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4425-6052T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052203 | |||||||
chr19:11052367 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4425-5888G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052367 | |||||||
chr19:11052585 | A | C | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-5670A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052585 | |||||||
chr19:11052590 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4425-5665C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052590 | |||||||
chr19:11052715 | G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-5540G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052715 | |||||||
chr19:11052720 | C | T | 2 | a0001c0018t0001g0039 a0001c0018t0001g0157 |
2 | NA18940.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.4425-5535C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052720 | |||||||
chr19:11052736 | C | G | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4425-5519C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052736 | |||||||
chr19:11052886 | C | T | 194 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0035 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.4425-5369C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052886 | |||||||
chr19:11052925 | G | T | 38 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0131 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-5330G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11052925 | |||||||
chr19:11053013 | A | G | 8 | a0001c0003t0001g0137 a0001c0003t0001g0210 a0001c0003t0001g0221 others(5): Show |
8 | HG01074.hp2 HG01168.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.4425-5242A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053013 | |||||||
chr19:11053119 | G | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0120 a0001c0001t0001g0170 others(2): Show |
5 | HG02922.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425-5136G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053119 | |||||||
chr19:11053138 | C | T | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4425-5117C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053138 | |||||||
chr19:11053148 | T | C | 68 | a0001c0002t0001g0208 a0001c0002t0001g0247 a0001c0002t0001g0251 others(65): Show |
68 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.4425-5107T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053148 | |||||||
chr19:11053171 | C | T | 102 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(99): Show |
102 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(99): Show |
intron_variant | MODIFIER | c.4425-5084C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053171 | |||||||
chr19:11053221 | T | C | 195 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.4425-5034T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053221 | |||||||
chr19:11053292 | T | C | 5 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(2): Show |
5 | HG02258.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4425-4963T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053292 | |||||||
chr19:11053372 | T | A | 1 | a0001c0002t0001g0236 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.4425-4883T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053372 | |||||||
chr19:11053379 | G | A | 4 | a0001c0011t0001g0276 a0001c0011t0001g0277 a0001c0011t0001g0278 others(1): Show |
4 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.4425-4876G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053379 | |||||||
chr19:11053391 | T | G | 194 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0035 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.4425-4864T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053391 | |||||||
chr19:11053451 | C | CA | 25 | a0001c0001t0001g0104 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4425-4787dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11053451 | ||||||
chr19:11053468 | AG | A | 8 | a0001c0001t0001g0064 a0001c0001t0001g0090 a0001c0002t0001g0218 others(5): Show |
8 | HG01257.hp2 HG03195.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.4425-4786delG | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053468 | |||||||
chr19:11053469 | G | A | 187 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0035 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.4425-4786G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053469 | |||||||
chr19:11053768 | A | G | 1 | a0001c0002t0001g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4425-4487A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053768 | |||||||
chr19:11053784 | G | A | 38 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0131 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-4471G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053784 | |||||||
chr19:11053830 | G | T | 2 | a0001c0004t0001g0025 a0001c0004t0001g0167 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4425-4425G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053830 | |||||||
chr19:11053867 | C | T | 1 | a0001c0002t0001g0252 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4425-4388C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053867 | |||||||
chr19:11053892 | C | A | 67 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0006 others(64): Show |
67 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.4425-4363C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053892 | |||||||
chr19:11053897 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4425-4358C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053897 | |||||||
chr19:11053991 | G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-4264G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11053991 | |||||||
chr19:11054021 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0166 a0001c0001t0001g0186 |
3 | HG01952.hp1 HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4425-4234C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054021 | |||||||
chr19:11054086 | G | A | 2 | a0001c0010t0001g0009 a0001c0010t0001g0010 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4425-4169G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054086 | |||||||
chr19:11054105 | A | G | 69 | a0001c0002t0001g0208 a0001c0002t0001g0247 a0001c0002t0001g0251 others(66): Show |
69 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.4425-4150A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054105 | |||||||
chr19:11054114 | A | G | 29 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0003t0001g0203 others(26): Show |
29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-4141A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054114 | |||||||
chr19:11054292 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4425-3963C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054292 | |||||||
chr19:11054292 | C | T | 122 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0035 others(119): Show |
122 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.4425-3963C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054292 | |||||||
chr19:11054376 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4425-3879A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054376 | |||||||
chr19:11054477 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4425-3778C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054477 | |||||||
chr19:11054604 | C | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0117 others(1): Show |
4 | NA18747.hp1 NA18948.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.4425-3651C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054604 | |||||||
chr19:11054634 | A | G | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4425-3621A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054634 | |||||||
chr19:11054746 | G | A | 1 | a0001c0007t0001g0018 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4425-3509G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054746 | |||||||
chr19:11054943 | G | A | 29 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0003t0001g0203 others(26): Show |
29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-3312G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054943 | |||||||
chr19:11054978 | C | T | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-3277C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11054978 | |||||||
chr19:11055090 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4425-3165C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055090 | |||||||
chr19:11055301 | T | C | 1 | a0001c0002t0001g0232 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4425-2954T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055301 | |||||||
chr19:11055315 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4425-2940G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055315 | |||||||
chr19:11055340 | T | C | 105 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(102): Show |
105 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.4425-2915T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055340 | |||||||
chr19:11055380 | G | T | 1 | a0001c0003t0001g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4425-2875G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055380 | |||||||
chr19:11055384 | A | G | 28 | a0001c0002t0001g0208 a0001c0003t0001g0203 a0001c0003t0001g0206 others(25): Show |
28 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4425-2871A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055384 | |||||||
chr19:11055487 | C | T | 34 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(31): Show |
34 | HG00544.hp2 HG01175.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.4425-2768C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055487 | |||||||
chr19:11055495 | G | T | 25 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0003t0001g0203 others(22): Show |
25 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4425-2760G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055495 | |||||||
chr19:11055617 | T | C | 101 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(98): Show |
101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.4425-2638T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055617 | |||||||
chr19:11055755 | CT | C | 38 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0131 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-2492delT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11055755 | ||||||
chr19:11055763 | T | C | 29 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0003t0001g0203 others(26): Show |
29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-2492T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055763 | |||||||
chr19:11055800 | T | C | 69 | a0001c0001t0001g0064 a0001c0001t0001g0134 a0001c0002t0001g0208 others(66): Show |
69 | HG00099.hp1 HG00544.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.4425-2455T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11055800 | |||||||
chr19:11056115 | A | G | 25 | a0001c0001t0001g0064 a0001c0001t0001g0102 a0001c0001t0001g0104 others(22): Show |
25 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.4425-2140A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056115 | |||||||
chr19:11056151 | G | A | 53 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0131 others(50): Show |
53 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.4425-2104G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056151 | |||||||
chr19:11056203 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0120 a0001c0001t0001g0170 others(2): Show |
5 | HG02922.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425-2052G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056203 | |||||||
chr19:11056317 | G | A | 1 | a0001c0015t0001g0023 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4425-1938G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056317 | |||||||
chr19:11056333 | A | C | 5 | a0001c0005t0001g0078 a0001c0005t0001g0242 a0001c0005t0001g0243 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425-1922A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056333 | |||||||
chr19:11056395 | A | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0120 a0001c0001t0001g0170 others(2): Show |
5 | HG02922.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425-1860A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056395 | |||||||
chr19:11056437 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0161 |
3 | HG02257.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.4425-1818C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056437 | |||||||
chr19:11056543 | C | T | 38 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0131 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-1712C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056543 | |||||||
chr19:11056764 | C | G | 35 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(32): Show |
35 | HG00544.hp2 HG01175.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.4425-1491C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056764 | |||||||
chr19:11056819 | A | G | 29 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0003t0001g0203 others(26): Show |
29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-1436A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056819 | |||||||
chr19:11056867 | C | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0046 |
2 | HG00597.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.4425-1388C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056867 | |||||||
chr19:11056905 | G | A | 23 | a0001c0003t0001g0006 a0001c0003t0001g0203 a0001c0003t0001g0206 others(20): Show |
23 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.4425-1350G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056905 | |||||||
chr19:11056936 | A | C | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-1319A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056936 | |||||||
chr19:11056953 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4425-1302G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056953 | |||||||
chr19:11056964 | C | T | 29 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0003t0001g0203 others(26): Show |
29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-1291C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056964 | |||||||
chr19:11056989 | C | T | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4425-1266C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11056989 | |||||||
chr19:11057043 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4425-1212A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057043 | |||||||
chr19:11057104 | T | C | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4425-1151T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057104 | |||||||
chr19:11057146 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4425-1109C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057146 | |||||||
chr19:11057324 | G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-931G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057324 | |||||||
chr19:11057330 | G | C | 1 | a0001c0003t0001g0253 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4425-925G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057330 | |||||||
chr19:11057353 | T | C | 67 | a0001c0002t0001g0208 a0001c0002t0001g0247 a0001c0002t0001g0251 others(64): Show |
67 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.4425-902T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057353 | |||||||
chr19:11057362 | A | G | 38 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0131 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4425-893A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057362 | |||||||
chr19:11057379 | G | A | 2 | a0001c0008t0001g0268 a0001c0008t0001g0269 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4425-876G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057379 | |||||||
chr19:11057453 | G | A | 1 | a0001c0015t0001g0023 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4425-802G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057453 | |||||||
chr19:11057539 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4425-716A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057539 | |||||||
chr19:11057585 | C | T | 42 | a0001c0002t0001g0247 a0001c0002t0001g0251 a0001c0003t0001g0006 others(39): Show |
42 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.4425-670C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057585 | |||||||
chr19:11057619 | C | T | 1 | a0001c0002t0001g0223 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4425-636C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057619 | |||||||
chr19:11057626 | G | C | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-629G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057626 | |||||||
chr19:11057874 | G | A | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4425-381G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057874 | |||||||
chr19:11057950 | A | G | 29 | a0001c0002t0001g0208 a0001c0003t0001g0006 a0001c0003t0001g0203 others(26): Show |
29 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4425-305A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11057950 | |||||||
chr19:11058028 | C | G | 3 | a0001c0004t0001g0025 a0001c0004t0001g0167 a0001c0028t0001g0007 |
3 | HG02257.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4425-227C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058028 | |||||||
chr19:11058093 | C | T | 15 | a0001c0003t0001g0203 a0001c0003t0001g0206 a0001c0003t0001g0209 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4425-162C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058093 | |||||||
chr19:11058106 | C | CA | 61 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0095 others(58): Show |
61 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.4425-136dupA | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr19 | 11058106 | ||||||
chr19:11058122 | G | A | 67 | a0001c0002t0001g0208 a0001c0002t0001g0247 a0001c0002t0001g0251 others(64): Show |
67 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.4425-133G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058122 | |||||||
chr19:11058185 | C | T | 1 | a0001c0003t0001g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4425-70C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058185 | |||||||
chr19:11058220 | A | G | 104 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(101): Show |
104 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(101): Show |
intron_variant | MODIFIER | c.4425-35A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 30/34 | chr19 | 11058220 | |||||||
chr19:11058385 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4533+22C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058385 | |||||||
chr19:11058393 | A | G | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4533+30A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058393 | |||||||
chr19:11058481 | G | T | 3 | a0001c0011t0001g0277 a0001c0011t0001g0278 a0001c0032t0001g0231 |
3 | HG02738.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4533+118G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058481 | |||||||
chr19:11058629 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0150 |
3 | HG00735.hp2 HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4534-159T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058629 | |||||||
chr19:11058705 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0126 a0001c0001t0001g0153 |
3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4534-83G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058705 | |||||||
chr19:11058705 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4534-83G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 31/34 | chr19 | 11058705 | |||||||
chr19:11058901 | G | A | 3 | a0001c0004t0001g0121 a0001c0004t0001g0160 a0001c0008t0001g0266 |
3 | HG02145.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4635+12G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11058901 | |||||||
chr19:11059230 | CTCTG | C | 15 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(12): Show |
15 | HG02145.hp1 HG02280.hp2 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.4635+347_4635+350d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr19 | 11059230 | ||||||
chr19:11059271 | T | C | 105 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(102): Show |
105 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.4635+382T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059271 | |||||||
chr19:11059487 | G | T | 2 | a0001c0001t0001g0152 a0001c0026t0001g0281 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4636-266G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059487 | |||||||
chr19:11059615 | C | T | 5 | a0001c0003t0001g0006 a0001c0004t0001g0025 a0001c0004t0001g0167 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4636-138C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059615 | |||||||
chr19:11059631 | G | A | 3 | a0001c0009t0001g0001 a0001c0009t0001g0002 a0001c0009t0001g0003 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4636-122G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059631 | |||||||
chr19:11059633 | A | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4636-120A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | chr19 | 11059633 | |||||||
chr19:11059684 | G | GGGGCCA | 5 | a0001c0004t0001g0121 a0001c0004t0001g0160 a0001c0008t0001g0266 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4636-63_4636-58dup others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr19 | 11059684 | ||||||
chr19:11059886 | G | C | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | splice_donor_variant&intron_variant | HIGH | c.4768+1G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059886 | |||||||
chr19:11059887 | T | A | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | splice_donor_variant&intron_variant | HIGH | c.4768+2T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059887 | |||||||
chr19:11059888 | G | C | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.4768+3G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059888 | |||||||
chr19:11059890 | G | C | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.4768+5G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059890 | |||||||
chr19:11059893 | C | T | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.4768+8C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059893 | |||||||
chr19:11059894 | C | A | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+9C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059894 | |||||||
chr19:11059895 | G | T | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+10G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059895 | |||||||
chr19:11059896 | G | C | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+11G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059896 | |||||||
chr19:11059897 | G | A | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+12G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059897 | |||||||
chr19:11059899 | G | A | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+14G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059899 | |||||||
chr19:11059900 | G | C | 2 | a0001c0003t0001g0224 a0001c0003t0001g0225 |
2 | HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4768+15G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059900 | |||||||
chr19:11059900 | G | T | 1 | a0003c0023t0001g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4768+15G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059900 | |||||||
chr19:11059901 | G | T | 6 | a0001c0002t0001g0080 a0001c0002t0001g0239 a0001c0006t0001g0270 others(3): Show |
6 | HG02451.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4768+16G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059901 | |||||||
chr19:11059909 | C | A | 1 | a0001c0002t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4768+24C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059909 | |||||||
chr19:11059983 | T | A | 4 | a0001c0003t0001g0006 a0001c0004t0001g0025 a0001c0004t0001g0167 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4769-62T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059983 | |||||||
chr19:11059987 | T | G | 1 | a0001c0004t0003g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4769-58T>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11059987 | |||||||
chr19:11060020 | G | A | 10 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(7): Show |
10 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4769-25G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 33/34 | chr19 | 11060020 | |||||||
chr19:11060239 | C | T | 1 | a0001c0025t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4911+52C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060239 | |||||||
chr19:11060287 | C | T | 10 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(7): Show |
10 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4911+100C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060287 | |||||||
chr19:11060306 | G | A | 11 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(8): Show |
11 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.4911+119G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060306 | |||||||
chr19:11060308 | G | A | 11 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(8): Show |
11 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.4911+121G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060308 | |||||||
chr19:11060310 | C | G | 11 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(8): Show |
11 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.4911+123C>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060310 | |||||||
chr19:11060334 | G | T | 10 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(7): Show |
10 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4911+147G>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060334 | |||||||
chr19:11060555 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.4911+368G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060555 | |||||||
chr19:11060605 | A | C | 62 | a0001c0003t0001g0131 a0001c0003t0001g0137 a0001c0003t0001g0149 others(59): Show |
62 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.4911+418A>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060605 | |||||||
chr19:11060642 | G | A | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4911+455G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060642 | |||||||
chr19:11060663 | T | A | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4911+476T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060663 | |||||||
chr19:11060780 | G | C | 5 | a0001c0004t0001g0121 a0001c0004t0001g0160 a0001c0008t0001g0266 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4911+593G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060780 | |||||||
chr19:11060808 | C | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4911+621C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060808 | |||||||
chr19:11060924 | T | C | 47 | a0001c0003t0001g0131 a0001c0003t0001g0137 a0001c0003t0001g0149 others(44): Show |
47 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.4911+737T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11060924 | |||||||
chr19:11061117 | G | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4912-667G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061117 | |||||||
chr19:11061148 | A | G | 10 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(7): Show |
10 | HG02698.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4912-636A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061148 | |||||||
chr19:11061185 | C | CT | 9 | a0001c0003t0001g0204 a0001c0003t0001g0217 a0001c0003t0001g0222 others(6): Show |
9 | HG02698.hp1 HG03942.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.4912-596dupT | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061185 | ||||||
chr19:11061188 | T | TAAAAAAA others(3): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0113 a0001c0002t0001g0263 |
3 | HG02280.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4912-588_4912-579d others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | ||||||
chr19:11061188 | T | TAAAAAAA others(4): Show |
1 | a0001c0028t0001g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4912-589_4912-579d others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | ||||||
chr19:11061188 | T | TAAAAAAA others(5): Show |
2 | a0001c0001t0001g0112 a0001c0016t0001g0230 |
2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4912-590_4912-579d others(14): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | ||||||
chr19:11061188 | T | TTA | 4 | a0001c0003t0001g0227 a0001c0004t0001g0167 a0001c0014t0001g0233 others(1): Show |
4 | HG00099.hp1 HG01515.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.4912-596_4912-595i others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061188 | |||||||
chr19:11061188 | TAA | T | 28 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0052 others(25): Show |
28 | HG00544.hp1 HG00621.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.4912-580_4912-579d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | ||||||
chr19:11061188 | TAAA | T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0062 others(3): Show |
6 | HG00558.hp2 HG01884.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.4912-581_4912-579d others(5): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | ||||||
chr19:11061188 | TAAAA | T | 15 | a0001c0001t0001g0085 a0001c0001t0001g0096 a0001c0001t0001g0097 others(12): Show |
15 | HG00735.hp2 HG01192.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.4912-582_4912-579d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061188 | ||||||
chr19:11061189 | A | T | 52 | a0001c0003t0001g0006 a0001c0003t0001g0131 a0001c0003t0001g0137 others(49): Show |
52 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.4912-595A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061189 | |||||||
chr19:11061196 | AAAAAAAA others(15): Show |
A | 16 | a0001c0003t0001g0203 a0001c0003t0001g0206 a0001c0003t0001g0209 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4912-586_4912-565d others(24): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061196 | ||||||
chr19:11061198 | AAAAAAAA others(15): Show |
A | 1 | a0001c0004t0001g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4912-584_4912-563d others(24): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061198 | ||||||
chr19:11061200 | A | T | 3 | a0001c0001t0001g0056 a0001c0003t0001g0204 a0001c0014t0001g0233 |
3 | HG01515.hp2 HG04184.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.4912-584A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061200 | |||||||
chr19:11061200 | AAAAAAT | A | 7 | a0001c0001t0001g0129 a0001c0001t0001g0152 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp1 HG02083.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.4912-582_4912-577d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061200 | ||||||
chr19:11061201 | AAAAAT | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG00558.hp1 HG01167.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.4912-581_4912-577d others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061201 | ||||||
chr19:11061202 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4912-581_4912-580i others(30): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | ||||||
chr19:11061202 | A | T | 10 | a0001c0001t0001g0049 a0001c0001t0001g0056 a0001c0001t0001g0057 others(7): Show |
10 | HG00099.hp1 HG01071.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.4912-582A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061202 | |||||||
chr19:11061202 | AAAAT | A | 49 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0038 others(46): Show |
49 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.4912-580_4912-577d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | ||||||
chr19:11061202 | AAAATAT | A | 22 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0106 others(19): Show |
22 | HG01192.hp1 HG01243.hp2 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.4912-580_4912-575d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | ||||||
chr19:11061202 | AAAATATA others(9): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4912-580_4912-565d others(18): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | ||||||
chr19:11061202 | AAAATATA others(13): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4912-580_4912-561d others(22): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061202 | ||||||
chr19:11061204 | A | AAAAAAAA others(31): Show |
1 | a0001c0002t0001g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(40): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAAAA others(26): Show |
1 | a0001c0002t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(35): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAAAA others(3): Show |
1 | a0001c0016t0001g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAAAA others(11): Show |
1 | a0001c0006t0001g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(20): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAAAA others(15): Show |
1 | a0001c0021t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(24): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAAAA others(13): Show |
1 | a0001c0030t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4912-579_4912-578i others(22): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAAAA others(23): Show |
2 | a0001c0006t0001g0270 a0001c0006t0001g0272 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4912-579_4912-578i others(32): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0168 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4912-579_4912-578i others(13): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAATA others(3): Show |
1 | a0001c0001t0001g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4912-579_4912-578i others(12): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | AAAAAATA others(7): Show |
1 | a0001c0002t0001g0146 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4912-579_4912-578i others(16): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | A | T | 34 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0047 others(31): Show |
34 | HG00099.hp1 HG00544.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.4912-580A>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061204 | |||||||
chr19:11061204 | AAT | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0075 a0001c0001t0001g0094 others(8): Show |
11 | HG00438.hp2 HG00673.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4912-543_4912-542d others(4): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | AATAT | A | 13 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0073 others(10): Show |
13 | HG01358.hp2 HG01981.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.4912-545_4912-542d others(6): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | AATATAT | A | 16 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0115 others(13): Show |
16 | HG00621.hp1 HG00673.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.4912-547_4912-542d others(8): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061204 | AATATATA others(11): Show |
A | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4912-559_4912-542d others(20): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr19 | 11061204 | ||||||
chr19:11061205 | ATATAT | A | 6 | a0001c0002t0001g0238 a0001c0007t0001g0017 a0001c0007t0001g0018 others(3): Show |
6 | HG01255.hp1 HG01516.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4912-578_4912-574d others(7): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061205 | |||||||
chr19:11061205 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-578_4912-562d others(19): Show |
SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061205 | |||||||
chr19:11061206 | T | A | 20 | a0001c0001t0001g0086 a0001c0001t0001g0112 a0001c0001t0001g0113 others(17): Show |
20 | HG02280.hp1 HG02698.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.4912-578T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061206 | |||||||
chr19:11061208 | T | A | 17 | a0001c0001t0001g0044 a0001c0001t0001g0112 a0001c0002t0001g0207 others(14): Show |
17 | HG00438.hp2 HG01175.hp2 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.4912-576T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061208 | |||||||
chr19:11061210 | T | A | 18 | a0001c0001t0001g0068 a0001c0001t0001g0091 a0001c0002t0001g0207 others(15): Show |
18 | HG01175.hp2 HG01981.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.4912-574T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061210 | |||||||
chr19:11061212 | T | A | 10 | a0001c0003t0001g0217 a0001c0003t0001g0222 a0001c0003t0001g0246 others(7): Show |
10 | HG02622.hp1 HG02698.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.4912-572T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061212 | |||||||
chr19:11061214 | T | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4912-570T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061214 | |||||||
chr19:11061216 | T | A | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4912-568T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061216 | |||||||
chr19:11061224 | T | A | 2 | a0001c0001t0001g0179 a0001c0031t0001g0008 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4912-560T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061224 | |||||||
chr19:11061226 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-558T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061226 | |||||||
chr19:11061228 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-556T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061228 | |||||||
chr19:11061230 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-554T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061230 | |||||||
chr19:11061232 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4912-552T>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061232 | |||||||
chr19:11061276 | C | A | 2 | a0001c0004t0001g0138 a0001c0008t0001g0266 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4912-508C>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061276 | |||||||
chr19:11061328 | T | C | 52 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(49): Show |
52 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.4912-456T>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061328 | |||||||
chr19:11061331 | G | A | 3 | a0001c0011t0001g0277 a0001c0011t0001g0278 a0001c0032t0001g0231 |
3 | HG02738.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4912-453G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061331 | |||||||
chr19:11061445 | G | A | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4912-339G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061445 | |||||||
chr19:11061494 | G | A | 1 | a0001c0022t0001g0201 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4912-290G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061494 | |||||||
chr19:11061537 | G | A | 1 | a0001c0031t0001g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4912-247G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061537 | |||||||
chr19:11061623 | G | A | 46 | a0001c0003t0001g0131 a0001c0003t0001g0137 a0001c0003t0001g0149 others(43): Show |
46 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.4912-161G>A | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061623 | |||||||
chr19:11061646 | G | C | 1 | a0001c0032t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4912-138G>C | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061646 | |||||||
chr19:11061671 | C | T | 1 | a0001c0004t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4912-113C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061671 | |||||||
chr19:11061679 | A | G | 1 | a0001c0004t0001g0191 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4912-105A>G | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061679 | |||||||
chr19:11061736 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4912-48C>T | SMARCA4 | ENSG00000127616.22 | transcript | ENST00000344626.10 | protein_coding | 34/34 | chr19 | 11061736 |