Item | Value |
---|---|
geneid | 3308 |
ensemblid | ENSG00000170606.16 |
hgncid | 5237 |
symbol | HSPA4 |
name | heat shock protein family A (Hsp70) member 4 |
refseq_nuc | NM_002154.4 |
refseq_prot | NP_002145.3 |
ensembl_nuc | ENST00000304858.7 |
ensembl_prot | ENSP00000302961.2 |
mane_status | MANE Select |
chr | chr5 |
start | 133052013 |
end | 133106449 |
strand | + |
ver | v1.2 |
region | chr5:133052013-133106449 |
region5000 | chr5:133047013-133111449 |
regionname0 | HSPA4_chr5_133052013_133106449 |
regionname5000 | HSPA4_chr5_133047013_133111449 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 840 | 349 | 82 | 68 | 153 | 12 | 32 | 116 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0002 | 0/0 | 840 | 4 | 1 | 2 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0003 | 0/0 | 840 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0004 | 0/0 | 840 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0005 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0006 | 0/0 | 840 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0007 | 0/0 | 840 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0008 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0009 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
a0010 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | MSVVG others(835): Show |
chr5 | 133047013 | 133111449 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2520 | 279 | 59 | 52 | 134 | 8 | 24 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0001c0002 | 0/0 | 2520 | 62 | 16 | 15 | 19 | 4 | 8 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0001c0004 | 0/0 | 2520 | 4 | 4 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0001c0007 | 0/0 | 2520 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0001c0011 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0001c0015 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0002c0003 | 0/0 | 2520 | 4 | 1 | 2 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0003c0005 | 0/0 | 2520 | 3 | 0 | 0 | 0 | 0 | 3 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0004c0006 | 0/0 | 2520 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0005c0009 | 0/0 | 2520 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0006c0012 | 0/0 | 2520 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0007c0008 | 0/0 | 2520 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0008c0013 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0009c0010 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 | ||
a0010c0014 | 0/0 | 2520 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | ATGTC others(2515): Show |
chr5 | 133047013 | 133111449 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4774 | 237 | 40 | 44 | 120 | 7 | 24 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0003 | 0/0 | 4773 | 8 | 5 | 3 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4768): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0004 | 0/0 | 4774 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0005 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4757): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0007 | 0/0 | 4774 | 4 | 0 | 0 | 4 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0008 | 0/0 | 4775 | 4 | 4 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4770): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0009 | 0/0 | 4774 | 4 | 2 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0010 | 0/0 | 4774 | 4 | 0 | 0 | 3 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0012 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0014 | 0/0 | 4775 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4770): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0015 | 0/0 | 4774 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0016 | 0/0 | 4774 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0019 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0020 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0021 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0022 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4757): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0023 | 0/0 | 4763 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4758): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0024 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0025 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0026 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0001t0036 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0002 | 0/0 | 4761 | 30 | 1 | 8 | 12 | 3 | 6 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4756): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0004 | 0/0 | 4774 | 6 | 6 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0005 | 0/0 | 4762 | 5 | 1 | 1 | 3 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4757): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0006 | 0/0 | 4774 | 5 | 4 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0013 | 0/0 | 4774 | 3 | 0 | 3 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0017 | 0/0 | 4761 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4756): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0018 | 0/0 | 4774 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0027 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0028 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0030 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0031 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0032 | 0/0 | 4774 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0033 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4757): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0034 | 0/0 | 4762 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4757): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0035 | 0/0 | 4761 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4756): Show |
chr5 | 133047013 | 133111449 |
a0001c0002t0037 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0004t0011 | 0/0 | 4774 | 3 | 3 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0004t0012 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0007t0001 | 0/0 | 4774 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0011t0001 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0001c0015t0012 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0002c0003t0001 | 0/0 | 4774 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0002c0003t0003 | 0/0 | 4773 | 2 | 0 | 1 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4768): Show |
chr5 | 133047013 | 133111449 |
a0003c0005t0001 | 0/0 | 4774 | 2 | 0 | 0 | 0 | 0 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0003c0005t0003 | 0/0 | 4773 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4768): Show |
chr5 | 133047013 | 133111449 |
a0004c0006t0001 | 0/0 | 4774 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0005c0009t0001 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0006c0012t0001 | 0/0 | 4774 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0007c0008t0029 | 0/0 | 4774 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0008c0013t0001 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4769): Show |
chr5 | 133047013 | 133111449 |
a0009c0010t0003 | 0/0 | 4773 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4768): Show |
chr5 | 133047013 | 133111449 |
a0010c0014t0003 | 0/0 | 4773 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | GAGAT others(4768): Show |
chr5 | 133047013 | 133111449 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0015g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0015g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0016g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0016g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0019g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0020g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0021g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0022g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0023g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0024g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0025g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0026g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0036g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0013g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0013g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0013g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0017g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0017g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0018g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0027g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0028g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0030g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0031g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0032g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0033g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0034g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0035g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0037g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0004t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0004t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0004t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0004t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0007t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0007t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0011t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0015t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0002c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0002c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0002c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0002c0003t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0003c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0003c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0003c0005t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0004c0006t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0004c0006t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0005c0009t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0006c0012t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0007c0008t0029g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0008c0013t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0009c0010t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0010c0014t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | GBR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0052 | EUR | GBR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00280 | hp1 | a0001 | c0001 | t0010 | g0283 | EUR | FIN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00323 | hp2 | a0001 | c0002 | t0032 | g0029 | EUR | FIN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00438 | hp2 | a0005 | c0009 | t0001 | g0291 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00609 | hp1 | a0001 | c0001 | t0019 | g0325 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00621 | hp2 | a0001 | c0002 | t0005 | g0070 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00639 | hp2 | a0001 | c0002 | t0013 | g0042 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00642 | hp2 | a0001 | c0002 | t0006 | g0054 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01069 | hp2 | a0001 | c0001 | t0009 | g0351 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0352 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0154 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01167 | hp2 | a0001 | c0002 | t0013 | g0026 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01168 | hp2 | a0001 | c0001 | t0016 | g0258 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01169 | hp1 | a0001 | c0002 | t0013 | g0058 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01169 | hp2 | a0001 | c0001 | t0016 | g0259 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01175 | hp1 | a0002 | c0003 | t0003 | g0161 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0076 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01256 | hp1 | a0001 | c0002 | t0018 | g0001 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01258 | hp2 | a0001 | c0002 | t0018 | g0001 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0072 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01496 | hp1 | a0001 | c0007 | t0001 | g0144 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0022 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01515 | hp1 | a0006 | c0012 | t0001 | g0285 | EUR | IBS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0067 | EUR | IBS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01516 | hp1 | a0007 | c0008 | t0029 | g0018 | EUR | IBS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0009 | EUR | IBS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01884 | hp1 | a0001 | c0002 | t0004 | g0075 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02027 | hp1 | a0001 | c0002 | t0017 | g0024 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02055 | hp2 | a0001 | c0004 | t0011 | g0014 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02056 | hp2 | a0001 | c0001 | t0025 | g0344 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0032 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02155 | hp2 | a0001 | c0001 | t0024 | g0243 | EAS | CDX | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02257 | hp2 | a0001 | c0002 | t0006 | g0059 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02258 | hp1 | a0004 | c0006 | t0001 | g0213 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0150 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02572 | hp2 | a0001 | c0002 | t0006 | g0053 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0353 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02615 | hp2 | a0008 | c0013 | t0001 | g0131 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0151 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02683 | hp2 | a0003 | c0005 | t0003 | g0166 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02698 | hp2 | a0002 | c0003 | t0003 | g0155 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02717 | hp2 | a0001 | c0002 | t0027 | g0055 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02735 | hp2 | a0001 | c0002 | t0035 | g0069 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02738 | hp1 | a0001 | c0002 | t0034 | g0041 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02886 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0056 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02896 | hp1 | a0001 | c0002 | t0005 | g0031 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02922 | hp1 | a0001 | c0004 | t0012 | g0012 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0003 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02965 | hp2 | a0001 | c0002 | t0004 | g0074 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02970 | hp1 | a0001 | c0004 | t0011 | g0011 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03098 | hp1 | a0001 | c0004 | t0011 | g0013 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0350 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03139 | hp1 | a0001 | c0015 | t0012 | g0016 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03195 | hp1 | a0001 | c0011 | t0001 | g0196 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03195 | hp2 | a0001 | c0007 | t0001 | g0153 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03209 | hp1 | a0001 | c0002 | t0037 | g0003 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03209 | hp2 | a0001 | c0002 | t0004 | g0057 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0231 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0152 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03516 | hp1 | a0001 | c0002 | t0028 | g0063 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0066 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04115 | hp2 | a0003 | c0005 | t0001 | g0169 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0065 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | CHB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18906 | hp1 | a0004 | c0006 | t0001 | g0242 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18940 | hp2 | a0001 | c0001 | t0010 | g0284 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18965 | hp2 | a0001 | c0002 | t0033 | g0064 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18975 | hp1 | a0001 | c0001 | t0007 | g0304 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18975 | hp2 | a0001 | c0001 | t0010 | g0281 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18987 | hp1 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18988 | hp1 | a0001 | c0001 | t0007 | g0235 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18988 | hp2 | a0001 | c0001 | t0010 | g0282 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18991 | hp2 | a0001 | c0001 | t0023 | g0113 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18993 | hp1 | a0001 | c0001 | t0007 | g0343 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18993 | hp2 | a0001 | c0001 | t0022 | g0106 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19043 | hp2 | a0001 | c0002 | t0006 | g0061 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19057 | hp1 | a0001 | c0002 | t0005 | g0044 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19060 | hp1 | a0001 | c0002 | t0017 | g0060 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19076 | hp1 | a0001 | c0002 | t0031 | g0025 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19082 | hp1 | a0001 | c0001 | t0020 | g0316 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19085 | hp2 | a0001 | c0002 | t0005 | g0049 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19088 | hp1 | a0001 | c0001 | t0021 | g0222 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19240 | hp2 | a0001 | c0001 | t0036 | g0015 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20129 | hp1 | a0001 | c0001 | t0012 | g0017 | AFR | ASW | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20129 | hp2 | a0009 | c0010 | t0003 | g0138 | AFR | ASW | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | TSI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20905 | hp1 | a0003 | c0005 | t0001 | g0174 | SAS | GIH | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | GIH | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02109 | hp2 | a0002 | c0003 | t0001 | g0182 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02486 | hp2 | a0001 | c0001 | t0026 | g0354 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02559 | hp2 | a0001 | c0001 | t0015 | g0301 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG06807 | hp1 | a0001 | c0002 | t0030 | g0028 | AFR | USA | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | USA | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | USA | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | USA | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0149 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA21309 | hp2 | a0010 | c0014 | t0003 | g0311 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0214 | REF | REF | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0233 | REF | REF | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:133052287 | T | A | 1 | a0007 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.37T>A | p.Cys13Ser | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/19 | 275/4774 | 37/2523 | 13/840 | chr5 | 133052287 | |||
chr5:133067417 | G | A | 1 | a0005 | 1 | HG00438.hp2 | missense_variant&splice_region_variant | MODERATE | c.166G>A | p.Val56Ile | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/19 | 404/4774 | 166/2523 | 56/840 | chr5 | 133067417 | |||
chr5:133070461 | G | A | 1 | a0004 | 2 | HG02258.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.394G>A | p.Val132Ile | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/19 | 632/4774 | 394/2523 | 132/840 | chr5 | 133070461 | |||
chr5:133073261 | G | A | 1 | a0009 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.461G>A | p.Arg154Gln | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/19 | 699/4774 | 461/2523 | 154/840 | chr5 | 133073261 | |||
chr5:133073275 | G | A | 1 | a0002 | 4 | HG01074.hp2 HG01175.hp1 HG02109.hp2 others(1): Show |
missense_variant | MODERATE | c.475G>A | p.Ala159Thr | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/19 | 713/4774 | 475/2523 | 159/840 | chr5 | 133073275 | |||
chr5:133076676 | C | T | 1 | a0010 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.686C>T | p.Thr229Met | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/19 | 924/4774 | 686/2523 | 229/840 | chr5 | 133076676 | |||
chr5:133092755 | C | T | 1 | a0008 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1616C>T | p.Pro539Leu | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/19 | 1854/4774 | 1616/2523 | 539/840 | chr5 | 133092755 | |||
chr5:133099561 | C | G | 1 | a0003 | 3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.1946C>G | p.Thr649Ser | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/19 | 2184/4774 | 1946/2523 | 649/840 | chr5 | 133099561 | |||
chr5:133104288 | C | T | 1 | a0006 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2375C>T | p.Pro792Leu | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 2613/4774 | 2375/2523 | 792/840 | chr5 | 133104288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:133052352 | C | T | 1 | a0001c0015 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.102C>T | p.Cys34Cys | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/19 | 340/4774 | 102/2523 | 34/840 | chr5 | 133052352 | |||
chr5:133073253 | A | G | 1 | a0001c0007 | 2 | HG01496.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.453A>G | p.Ala151Ala | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/19 | 691/4774 | 453/2523 | 151/840 | chr5 | 133073253 | |||
chr5:133074057 | A | C | 1 | a0001c0004 | 4 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.594A>C | p.Val198Val | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/19 | 832/4774 | 594/2523 | 198/840 | chr5 | 133074057 | |||
chr5:133076816 | T | C | 1 | a0001c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.826T>C | p.Leu276Leu | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/19 | 1064/4774 | 826/2523 | 276/840 | chr5 | 133076816 | |||
chr5:133101839 | C | T | 1 | a0001c0002 | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
synonymous_variant | LOW | c.2118C>T | p.Ile706Ile | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/19 | 2356/4774 | 2118/2523 | 706/840 | chr5 | 133101839 | |||
chr5:133104289 | T | C | 1 | a0006c0012 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.2376T>C | p.Pro792Pro | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 2614/4774 | 2376/2523 | 792/840 | chr5 | 133104289 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:133052032 | C | A | 1 | a0001c0001t0014 | 2 | HG02280.hp2 HG02630.hp1 |
5_prime_UTR_variant | MODIFIER | c.-219C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/19 | 219 | chr5 | 133052032 | ||||||
chr5:133052041 | C | T | 1 | a0001c0002t0037 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-210C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/19 | 210 | chr5 | 133052041 | ||||||
chr5:133104512 | C | T | 1 | a0001c0001t0036 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 76 | chr5 | 133104512 | ||||||
chr5:133104576 | A | C | 1 | a0001c0001t0010 | 4 | HG00280.hp1 NA18940.hp2 NA18975.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*140A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 140 | chr5 | 133104576 | ||||||
chr5:133104593 | C | G | 25 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(22): Show |
76 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 157 | chr5 | 133104593 | ||||||
chr5:133104731 | T | C | 1 | a0001c0002t0027 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 295 | chr5 | 133104731 | ||||||
chr5:133104905 | C | T | 1 | a0001c0001t0016 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*469C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 469 | chr5 | 133104905 | ||||||
chr5:133104935 | G | A | 1 | a0001c0001t0019 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*499G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 499 | chr5 | 133104935 | ||||||
chr5:133105064 | G | GT | 2 | a0001c0001t0008 a0001c0001t0014 |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*629dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 630 | INFO_REALIGN_3_PRIME | chr5 | 133105064 | |||||
chr5:133105296 | G | A | 1 | a0001c0001t0015 | 2 | HG02559.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*860G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 860 | chr5 | 133105296 | ||||||
chr5:133105301 | G | A | 1 | a0001c0001t0020 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 865 | chr5 | 133105301 | ||||||
chr5:133105386 | C | T | 1 | a0001c0002t0035 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*950C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 950 | chr5 | 133105386 | ||||||
chr5:133105511 | C | T | 1 | a0001c0001t0026 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1075 | chr5 | 133105511 | ||||||
chr5:133105578 | T | C | 1 | a0001c0002t0028 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1142 | chr5 | 133105578 | ||||||
chr5:133105581 | T | A | 1 | a0001c0002t0035 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1145T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1145 | chr5 | 133105581 | ||||||
chr5:133105610 | A | G | 19 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(16): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1174A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1174 | chr5 | 133105610 | ||||||
chr5:133105766 | A | G | 1 | a0001c0002t0034 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1330 | chr5 | 133105766 | ||||||
chr5:133105782 | A | T | 1 | a0001c0001t0007 | 4 | NA18975.hp1 NA18987.hp1 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1346A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1346 | chr5 | 133105782 | ||||||
chr5:133105783 | T | A | 1 | a0001c0001t0007 | 4 | NA18975.hp1 NA18987.hp1 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1347T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1347 | chr5 | 133105783 | ||||||
chr5:133105788 | C | T | 1 | a0001c0001t0025 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1352C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1352 | chr5 | 133105788 | ||||||
chr5:133105801 | C | T | 1 | a0001c0001t0024 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1365C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1365 | chr5 | 133105801 | ||||||
chr5:133105811 | T | G | 1 | a0001c0002t0017 | 2 | HG02027.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1375T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1375 | chr5 | 133105811 | ||||||
chr5:133106089 | TA | T | 5 | a0001c0001t0003 a0002c0003t0003 a0003c0005t0003 others(2): Show |
13 | HG01175.hp1 HG01258.hp1 HG01346.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1666delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | INFO_REALIGN_3_PRIME | chr5 | 133106089 | |||||
chr5:133106100 | AAATTTTT others(4): Show |
A | 1 | a0001c0001t0023 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1665_*1675delAATT others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1665 | chr5 | 133106100 | ||||||
chr5:133106100 | AAATTTTT others(5): Show |
A | 1 | a0001c0001t0022 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1665_*1676delAATT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1665 | chr5 | 133106100 | ||||||
chr5:133106101 | A | AT | 1 | a0001c0001t0001 | 3 | HG01952.hp1 HG02896.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1665_*1666insT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AAT | A | 5 | a0001c0001t0001 a0001c0001t0008 a0001c0007t0001 others(2): Show |
11 | HG01099.hp1 HG01106.hp1 HG01496.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1667delAT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATT | A | 2 | a0001c0001t0001 a0001c0001t0008 |
6 | HG01070.hp1 HG01071.hp1 HG01981.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1668delATT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(3): Show |
A | 1 | a0001c0001t0001 | 6 | HG02056.hp1 NA18953.hp1 NA18995.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1675delATTT others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(4): Show |
A | 1 | a0001c0001t0001 | 32 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1676delATTT others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(5): Show |
A | 1 | a0001c0001t0001 | 2 | HG03225.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1677delATTT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(6): Show |
A | 1 | a0001c0001t0001 | 3 | HG02109.hp1 HG03486.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1678delATTT others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(7): Show |
A | 1 | a0001c0002t0030 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666_*1679delATTT others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(8): Show |
A | 2 | a0001c0001t0014 a0001c0002t0031 |
2 | HG02280.hp2 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1680delATTT others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(9): Show |
A | 2 | a0001c0001t0001 a0001c0001t0014 |
2 | HG01167.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1681delATTT others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(10): Show |
A | 3 | a0001c0001t0001 a0001c0001t0026 a0008c0013t0001 |
6 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1682delATTT others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(11): Show |
A | 1 | a0001c0001t0001 | 3 | HG03041.hp2 NA18972.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1683delATTT others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(12): Show |
A | 1 | a0001c0002t0013 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666_*1684delATTT others(15): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(13): Show |
A | 1 | a0001c0001t0001 | 2 | HG01243.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1685delATTT others(16): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106101 | AATTTTTT others(14): Show |
A | 1 | a0001c0001t0001 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666_*1686delATTT others(17): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | ||||||
chr5:133106102 | A | AT | 6 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0015 others(3): Show |
30 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1704dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | A | ATT | 3 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0020 |
21 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1703_*1704dupTT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | A | ATTT | 1 | a0001c0001t0001 | 10 | HG00140.hp2 HG02074.hp2 HG02132.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1702_*1704dupTTT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1693_*1704dupTTTT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1690_*1704dupTTTT others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | A | T | 1 | a0001c0001t0001 | 18 | HG01106.hp2 HG01952.hp1 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1666A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106102 | ||||||
chr5:133106102 | AT | A | 3 | a0001c0001t0001 a0001c0001t0016 a0006c0012t0001 |
11 | HG00408.hp2 HG01123.hp1 HG01168.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1704delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1704 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTT | A | 2 | a0001c0001t0001 a0001c0001t0025 |
6 | HG02056.hp2 HG03017.hp2 HG03492.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1700_*1704delTTTT others(1): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1700 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTT | A | 2 | a0001c0001t0001 a0001c0001t0007 |
20 | HG00099.hp1 HG00408.hp1 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1699_*1704delTTTT others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1699 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT | A | 4 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0021 others(1): Show |
27 | HG00639.hp1 HG01069.hp1 HG01192.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1698_*1704delTTTT others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1698 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT others(3): Show |
A | 1 | a0001c0004t0011 | 3 | HG02055.hp2 HG02970.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1695_*1704delTTTT others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1695 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT others(4): Show |
A | 6 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0036 others(3): Show |
7 | HG01516.hp1 HG02523.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1694_*1704delTTTT others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1694 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693_*1704delTTTT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1693 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1692_*1704delTTTT others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1692 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0019 a0001c0002t0006 a0001c0002t0018 |
8 | HG00609.hp1 HG00642.hp2 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1691_*1704delTTTT others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1691 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT others(8): Show |
A | 6 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0027 others(3): Show |
11 | HG00323.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1690_*1704delTTTT others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1690 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1689_*1704delTTTT others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1689 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106102 | ATTTTTTT others(11): Show |
A | 1 | a0001c0002t0013 | 2 | HG00639.hp2 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1687_*1704delTTTT others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1687 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | |||||
chr5:133106103 | T | A | 1 | a0001c0001t0005 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1667 | chr5 | 133106103 | ||||||
chr5:133106105 | T | G | 6 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0017 others(3): Show |
40 | HG00140.hp1 HG00621.hp2 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1669T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1669 | chr5 | 133106105 | ||||||
chr5:133106106 | T | G | 1 | a0001c0001t0005 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1670T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1670 | chr5 | 133106106 | ||||||
chr5:133106108 | T | A | 1 | a0001c0001t0001 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1672 | chr5 | 133106108 | ||||||
chr5:133106108 | T | G | 6 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0017 others(3): Show |
40 | HG00140.hp1 HG00621.hp2 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1672T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1672 | chr5 | 133106108 | ||||||
chr5:133106109 | T | A | 1 | a0001c0001t0001 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1673T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1673 | chr5 | 133106109 | ||||||
chr5:133106109 | T | G | 1 | a0001c0001t0005 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1673T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1673 | chr5 | 133106109 | ||||||
chr5:133106115 | T | G | 1 | a0001c0004t0011 | 3 | HG02055.hp2 HG02970.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1679T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1679 | chr5 | 133106115 | ||||||
chr5:133106116 | T | G | 4 | a0001c0001t0012 a0001c0001t0036 a0001c0004t0012 others(1): Show |
4 | HG02922.hp1 HG03139.hp1 NA19240.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1680T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1680 | chr5 | 133106116 | ||||||
chr5:133106117 | T | A | 1 | a0001c0001t0019 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1681T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1681 | chr5 | 133106117 | ||||||
chr5:133106118 | T | G | 1 | a0001c0002t0030 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1682T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1682 | chr5 | 133106118 | ||||||
chr5:133106119 | T | G | 3 | a0001c0002t0006 a0001c0002t0018 a0001c0002t0031 |
8 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1683T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1683 | chr5 | 133106119 | ||||||
chr5:133106120 | T | G | 6 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0027 others(3): Show |
11 | HG00323.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1684T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1684 | chr5 | 133106120 | ||||||
chr5:133106121 | T | G | 1 | a0001c0002t0030 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1685 | chr5 | 133106121 | ||||||
chr5:133106122 | T | G | 3 | a0001c0002t0006 a0001c0002t0018 a0001c0002t0031 |
8 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1686T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1686 | chr5 | 133106122 | ||||||
chr5:133106123 | T | G | 7 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0013 others(4): Show |
14 | HG00323.hp2 HG00639.hp2 HG01167.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1687T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1687 | chr5 | 133106123 | ||||||
chr5:133106125 | T | G | 1 | a0001c0002t0018 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1689T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1689 | chr5 | 133106125 | ||||||
chr5:133106126 | T | G | 5 | a0001c0002t0002 a0001c0002t0017 a0001c0002t0032 others(2): Show |
35 | HG00140.hp1 HG00323.hp2 HG01081.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1690T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1690 | chr5 | 133106126 | ||||||
chr5:133106127 | T | G | 6 | a0001c0001t0005 a0001c0002t0002 a0001c0002t0005 others(3): Show |
40 | HG00140.hp1 HG00621.hp2 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1691T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1691 | chr5 | 133106127 | ||||||
chr5:133106128 | T | G | 4 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0033 others(1): Show |
8 | HG00621.hp2 HG01496.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1692T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1692 | chr5 | 133106128 | ||||||
chr5:133106128 | TTTTTTTT others(6): Show |
T | 3 | a0001c0002t0002 a0001c0002t0017 a0001c0002t0035 |
33 | HG00140.hp1 HG01081.hp1 HG01255.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1693_*1705delTTTT others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1693 | chr5 | 133106128 | ||||||
chr5:133106129 | TTTTTTTT others(5): Show |
T | 4 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0033 others(1): Show |
8 | HG00621.hp2 HG01496.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1694_*1705delTTTT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1694 | chr5 | 133106129 | ||||||
chr5:133106133 | T | G | 1 | a0001c0001t0001 | 2 | NA18953.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1697T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1697 | chr5 | 133106133 | ||||||
chr5:133106134 | T | G | 1 | a0001c0001t0001 | 2 | NA18953.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1698T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1698 | chr5 | 133106134 | ||||||
chr5:133106135 | T | G | 3 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0023 |
41 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1699T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1699 | chr5 | 133106135 | ||||||
chr5:133106136 | T | G | 3 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0023 |
44 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1700T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1700 | chr5 | 133106136 | ||||||
chr5:133106137 | T | G | 1 | a0001c0001t0001 | 5 | HG01243.hp2 HG02280.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1701T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1701 | chr5 | 133106137 | ||||||
chr5:133106138 | T | G | 3 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0023 |
49 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1702T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1702 | chr5 | 133106138 | ||||||
chr5:133106139 | T | G | 1 | a0001c0002t0030 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1703T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1703 | chr5 | 133106139 | ||||||
chr5:133106140 | T | G | 4 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0023 others(1): Show |
50 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1704T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1704 | chr5 | 133106140 | ||||||
chr5:133106141 | G | GGT | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(11): Show |
33 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1725_*1726dupTG | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1727 | INFO_REALIGN_3_PRIME | chr5 | 133106141 | |||||
chr5:133106141 | G | GGTGTGT | 6 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0026 others(3): Show |
12 | HG01074.hp2 HG01167.hp1 HG01175.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1721_*1726dupTGTG others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1727 | INFO_REALIGN_3_PRIME | chr5 | 133106141 | |||||
chr5:133106141 | G | T | 4 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0023 others(1): Show |
50 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1705G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | chr5 | 133106141 | ||||||
chr5:133106158 | G | T | 1 | a0001c0001t0021 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1722G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1722 | chr5 | 133106158 | ||||||
chr5:133106165 | G | A | 1 | a0001c0002t0031 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1729 | chr5 | 133106165 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:133052376 | T | G | 72 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0008g0019 others(69): Show |
74 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+19T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052376 | |||||||
chr5:133052395 | A | G | 1 | a0001c0001t0001g0356 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.107+38A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052395 | |||||||
chr5:133052520 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.107+163G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052520 | |||||||
chr5:133052615 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.107+258G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052615 | |||||||
chr5:133052801 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.107+444T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052801 | |||||||
chr5:133052824 | C | T | 1 | a0001c0001t0001g0355 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.107+467C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052824 | |||||||
chr5:133052825 | G | T | 1 | a0001c0001t0001g0355 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.107+468G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052825 | |||||||
chr5:133052869 | G | A | 2 | a0001c0002t0002g0009 a0001c0002t0002g0010 |
2 | HG01256.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.107+512G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052869 | |||||||
chr5:133052980 | A | G | 1 | a0001c0001t0026g0354 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107+623A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052980 | |||||||
chr5:133053047 | G | C | 1 | a0001c0001t0001g0356 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.107+690G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053047 | |||||||
chr5:133053055 | C | G | 1 | a0001c0001t0004g0076 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.107+698C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053055 | |||||||
chr5:133053104 | C | T | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+747C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053104 | |||||||
chr5:133053107 | C | G | 1 | a0001c0001t0001g0349 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.107+750C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053107 | |||||||
chr5:133053213 | A | G | 1 | a0001c0001t0001g0348 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+856A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053213 | |||||||
chr5:133053267 | C | T | 62 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(59): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.107+910C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053267 | |||||||
chr5:133053268 | G | A | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.107+911G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053268 | |||||||
chr5:133053323 | C | CTAT | 55 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0027 others(52): Show |
57 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.107+967_107+968ins others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133053323 | ||||||
chr5:133053325 | C | A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0080 others(128): Show |
132 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.107+968C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053325 | |||||||
chr5:133053328 | C | CT | 40 | a0001c0001t0001g0004 a0001c0001t0001g0159 a0001c0001t0001g0160 others(37): Show |
41 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.107+990dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133053328 | ||||||
chr5:133053328 | C | T | 55 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0027 others(52): Show |
57 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.107+971C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053328 | |||||||
chr5:133053328 | CT | C | 9 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0185 others(6): Show |
9 | HG01099.hp2 HG02055.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.107+990delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133053328 | ||||||
chr5:133053540 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02132.hp1 HG02135.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.107+1183G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053540 | |||||||
chr5:133053550 | A | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.107+1193A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053550 | |||||||
chr5:133053587 | C | T | 62 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(59): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.107+1230C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053587 | |||||||
chr5:133053693 | C | G | 1 | a0001c0007t0001g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.107+1336C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053693 | |||||||
chr5:133053827 | A | G | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+1470A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053827 | |||||||
chr5:133053850 | G | A | 1 | a0001c0001t0001g0355 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.107+1493G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053850 | |||||||
chr5:133053893 | C | T | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+1536C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053893 | |||||||
chr5:133053995 | C | G | 60 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.107+1638C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053995 | |||||||
chr5:133054054 | C | CA | 56 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(53): Show |
58 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.107+1698dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133054054 | ||||||
chr5:133054569 | T | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.107+2212T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133054569 | |||||||
chr5:133054623 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+2266C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133054623 | |||||||
chr5:133054887 | G | C | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+2530G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133054887 | |||||||
chr5:133054891 | T | C | 62 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(59): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.107+2534T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133054891 | |||||||
chr5:133055014 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.107+2657T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055014 | |||||||
chr5:133055060 | G | T | 148 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(145): Show |
151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.107+2703G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055060 | |||||||
chr5:133055196 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.107+2839T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055196 | |||||||
chr5:133055200 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.107+2843G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055200 | |||||||
chr5:133055218 | A | G | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+2861A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055218 | |||||||
chr5:133055247 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.107+2890C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055247 | |||||||
chr5:133055307 | A | AT | 58 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0177 others(55): Show |
59 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.107+2981dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | A | ATT | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0085 others(7): Show |
10 | HG01175.hp2 HG01346.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+2980_107+2981d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | A | ATTTTTTT others(13): Show |
1 | a0002c0003t0001g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107+2962_107+2981d others(22): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | AT | A | 22 | a0001c0001t0001g0086 a0001c0001t0001g0159 a0001c0001t0001g0160 others(19): Show |
22 | HG00642.hp1 HG01069.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+2981delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | ATT | A | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0146 others(5): Show |
8 | HG01074.hp2 HG01496.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+2980_107+2981d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | ATTT | A | 8 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
8 | HG02109.hp1 HG02647.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+2979_107+2981d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | ATTTT | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG02486.hp2 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+2978_107+2981d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | ATTTTT | A | 34 | a0001c0001t0001g0084 a0001c0001t0001g0115 a0001c0001t0001g0116 others(31): Show |
35 | HG00621.hp2 HG01167.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.107+2977_107+2981d others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | ATTTTTT | A | 75 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0083 others(72): Show |
76 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.107+2976_107+2981d others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | ATTTTTTT | A | 13 | a0001c0001t0001g0087 a0001c0001t0008g0020 a0001c0001t0014g0150 others(10): Show |
13 | HG00323.hp2 HG01167.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.107+2975_107+2981d others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0008g0019 a0001c0001t0008g0149 a0001c0001t0009g0350 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+2974_107+2981d others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055307 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.107+2972_107+2981d others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | ||||||
chr5:133055357 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+3000A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055357 | |||||||
chr5:133055618 | A | C | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.107+3261A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055618 | |||||||
chr5:133055644 | A | G | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+3287A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055644 | |||||||
chr5:133055730 | A | G | 56 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(53): Show |
58 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.107+3373A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055730 | |||||||
chr5:133055770 | C | T | 63 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(60): Show |
65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.107+3413C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055770 | |||||||
chr5:133055946 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+3589C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055946 | |||||||
chr5:133055950 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0335 |
2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.107+3593C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055950 | |||||||
chr5:133055961 | C | T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG01167.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+3604C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055961 | |||||||
chr5:133055992 | C | T | 2 | a0001c0001t0004g0076 a0001c0001t0005g0021 |
2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.107+3635C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055992 | |||||||
chr5:133055993 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.107+3636G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055993 | |||||||
chr5:133056009 | T | C | 153 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(150): Show |
156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.107+3652T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056009 | |||||||
chr5:133056010 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.107+3653G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056010 | |||||||
chr5:133056335 | A | AT | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.107+3983dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133056335 | ||||||
chr5:133056372 | C | T | 1 | a0001c0002t0002g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107+4015C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056372 | |||||||
chr5:133056380 | C | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.107+4023C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056380 | |||||||
chr5:133056443 | T | C | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107+4086T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056443 | |||||||
chr5:133056642 | A | G | 1 | a0001c0007t0001g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.107+4285A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056642 | |||||||
chr5:133056701 | A | G | 152 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(149): Show |
155 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.107+4344A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056701 | |||||||
chr5:133056799 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.107+4442A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056799 | |||||||
chr5:133056835 | C | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+4478C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056835 | |||||||
chr5:133057048 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0023g0113 |
2 | NA18989.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.107+4691A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057048 | |||||||
chr5:133057102 | A | G | 3 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 |
3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107+4745A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057102 | |||||||
chr5:133057205 | G | A | 2 | a0002c0003t0001g0154 a0002c0003t0003g0155 |
2 | HG01074.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.107+4848G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057205 | |||||||
chr5:133057356 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.107+4999G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057356 | |||||||
chr5:133057360 | C | CT | 61 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0082 others(58): Show |
61 | HG00558.hp1 HG00609.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.107+5019dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133057360 | ||||||
chr5:133057360 | C | CTT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0183 others(3): Show |
7 | HG00438.hp1 HG03225.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+5018_107+5019d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133057360 | ||||||
chr5:133057415 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.107+5058A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057415 | |||||||
chr5:133057515 | C | T | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+5158C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057515 | |||||||
chr5:133057531 | C | G | 63 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0077 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.107+5174C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057531 | |||||||
chr5:133057550 | A | G | 4 | a0001c0002t0004g0003 a0001c0002t0004g0074 a0001c0002t0004g0075 others(1): Show |
4 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+5193A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057550 | |||||||
chr5:133057584 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0184 |
3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.107+5227T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057584 | |||||||
chr5:133057615 | A | G | 2 | a0001c0002t0018g0001 a0001c0002t0032g0029 |
3 | HG00323.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.107+5258A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057615 | |||||||
chr5:133057648 | A | G | 66 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.107+5291A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057648 | |||||||
chr5:133057697 | A | G | 60 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.107+5340A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057697 | |||||||
chr5:133058071 | A | C | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.107+5714A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058071 | |||||||
chr5:133058115 | G | A | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107+5758G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058115 | |||||||
chr5:133058134 | G | C | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.107+5777G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058134 | |||||||
chr5:133058143 | G | A | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+5786G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058143 | |||||||
chr5:133058156 | C | T | 1 | a0001c0007t0001g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.107+5799C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058156 | |||||||
chr5:133058404 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
5 | HG00099.hp2 HG00323.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+6047A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058404 | |||||||
chr5:133058495 | C | G | 1 | a0001c0001t0003g0175 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.107+6138C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058495 | |||||||
chr5:133058539 | G | A | 1 | a0001c0002t0005g0031 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.107+6182G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058539 | |||||||
chr5:133058603 | G | A | 3 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 |
3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107+6246G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058603 | |||||||
chr5:133058678 | C | G | 10 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0171 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-6302C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058678 | |||||||
chr5:133058849 | C | T | 1 | a0001c0002t0002g0073 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108-6131C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058849 | |||||||
chr5:133058930 | C | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(53): Show |
57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.108-6050C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058930 | |||||||
chr5:133059001 | G | A | 2 | a0001c0002t0004g0033 a0001c0002t0006g0032 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.108-5979G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059001 | |||||||
chr5:133059033 | CAGG | C | 29 | a0001c0001t0001g0085 a0001c0001t0001g0159 a0001c0001t0001g0162 others(26): Show |
29 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.108-5944_108-5942d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133059033 | ||||||
chr5:133059138 | A | G | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-5842A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059138 | |||||||
chr5:133059189 | T | C | 10 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0171 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-5791T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059189 | |||||||
chr5:133059222 | C | T | 4 | a0001c0001t0010g0281 a0001c0001t0010g0282 a0001c0001t0010g0283 others(1): Show |
4 | HG00280.hp1 NA18940.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-5758C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059222 | |||||||
chr5:133059447 | C | CA | 105 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0083 others(102): Show |
107 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.108-5517dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133059447 | ||||||
chr5:133059447 | C | CAA | 7 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG02027.hp1 HG04184.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-5518_108-5517d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133059447 | ||||||
chr5:133059447 | CA | C | 12 | a0001c0001t0001g0140 a0001c0001t0001g0181 a0001c0001t0001g0318 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.108-5517delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133059447 | ||||||
chr5:133059645 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.108-5335A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059645 | |||||||
chr5:133059688 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.108-5292G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059688 | |||||||
chr5:133059692 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.108-5288C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059692 | |||||||
chr5:133059845 | T | G | 90 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(87): Show |
92 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.108-5135T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059845 | |||||||
chr5:133059874 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108-5106C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059874 | |||||||
chr5:133059883 | A | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0345 |
2 | HG01074.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.108-5097A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059883 | |||||||
chr5:133060030 | T | C | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108-4950T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060030 | |||||||
chr5:133060048 | A | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-4932A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060048 | |||||||
chr5:133060068 | C | CTTT | 64 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(61): Show |
66 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.108-4903_108-4901d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060068 | ||||||
chr5:133060068 | C | CTTTTT | 112 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0080 others(109): Show |
113 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.108-4905_108-4901d others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060068 | ||||||
chr5:133060111 | G | A | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-4869G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060111 | |||||||
chr5:133060191 | T | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(53): Show |
57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.108-4789T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060191 | |||||||
chr5:133060201 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.108-4779T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060201 | |||||||
chr5:133060264 | G | A | 4 | a0001c0002t0002g0035 a0001c0002t0002g0036 a0001c0002t0002g0037 others(1): Show |
4 | NA18960.hp1 NA18994.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-4716G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060264 | |||||||
chr5:133060410 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.108-4570C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060410 | |||||||
chr5:133060440 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(150): Show |
156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.108-4540A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060440 | |||||||
chr5:133060607 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.108-4373C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060607 | |||||||
chr5:133060659 | G | A | 1 | a0001c0002t0002g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.108-4321G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060659 | |||||||
chr5:133060816 | C | CT | 88 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0083 others(85): Show |
91 | HG00140.hp1 HG00621.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.108-4143dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060816 | ||||||
chr5:133060816 | C | CTT | 62 | a0001c0001t0001g0078 a0001c0001t0001g0088 a0001c0001t0001g0090 others(59): Show |
62 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.108-4144_108-4143d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060816 | ||||||
chr5:133060816 | CT | C | 8 | a0001c0001t0001g0080 a0001c0001t0001g0209 a0001c0001t0001g0210 others(5): Show |
8 | HG01074.hp2 HG01168.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-4143delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060816 | ||||||
chr5:133060836 | T | TC | 4 | a0001c0004t0011g0011 a0001c0004t0011g0013 a0001c0004t0011g0014 others(1): Show |
4 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-4144_108-4143i others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060836 | |||||||
chr5:133060851 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.108-4129G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060851 | |||||||
chr5:133061088 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.108-3892G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061088 | |||||||
chr5:133061110 | C | T | 3 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 |
3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.108-3870C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061110 | |||||||
chr5:133061115 | G | C | 1 | a0001c0002t0002g0038 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.108-3865G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061115 | |||||||
chr5:133061125 | CT | C | 7 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0001t0001g0256 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-3840delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133061125 | ||||||
chr5:133061270 | C | T | 1 | a0001c0002t0002g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.108-3710C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061270 | |||||||
chr5:133061278 | A | G | 90 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(87): Show |
92 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.108-3702A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061278 | |||||||
chr5:133061358 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.108-3622G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061358 | |||||||
chr5:133061401 | T | C | 1 | a0001c0001t0026g0354 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108-3579T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061401 | |||||||
chr5:133061429 | C | CTACT | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-3549_108-3548i others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133061429 | ||||||
chr5:133061429 | C | CTATT | 83 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(80): Show |
85 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.108-3549_108-3548i others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133061429 | ||||||
chr5:133061549 | A | G | 23 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(20): Show |
23 | HG01496.hp1 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.108-3431A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061549 | |||||||
chr5:133061659 | G | A | 3 | a0001c0002t0002g0040 a0001c0002t0002g0072 a0001c0002t0005g0022 |
3 | HG01081.hp1 HG01361.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.108-3321G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061659 | |||||||
chr5:133061898 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-3082T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061898 | |||||||
chr5:133061924 | G | A | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-3056G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061924 | |||||||
chr5:133061930 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.108-3050G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061930 | |||||||
chr5:133061958 | T | C | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108-3022T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061958 | |||||||
chr5:133061975 | G | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(53): Show |
57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.108-3005G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061975 | |||||||
chr5:133062006 | A | T | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-2974A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062006 | |||||||
chr5:133062013 | G | A | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108-2967G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062013 | |||||||
chr5:133062397 | C | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.108-2583C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062397 | |||||||
chr5:133062431 | A | T | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-2549A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062431 | |||||||
chr5:133062437 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.108-2543G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062437 | |||||||
chr5:133062669 | T | C | 1 | a0001c0002t0005g0031 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.108-2311T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062669 | |||||||
chr5:133062676 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.108-2304C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062676 | |||||||
chr5:133062898 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.108-2082T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062898 | |||||||
chr5:133062912 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0183 |
2 | NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.108-2068A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062912 | |||||||
chr5:133062939 | G | T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108-2041G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062939 | |||||||
chr5:133063100 | CT | C | 31 | a0001c0001t0001g0085 a0001c0001t0001g0159 a0001c0001t0001g0160 others(28): Show |
31 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.108-1870delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133063100 | ||||||
chr5:133063112 | A | C | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-1868A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063112 | |||||||
chr5:133063289 | A | AT | 66 | a0001c0001t0001g0314 a0001c0001t0004g0076 a0001c0001t0005g0021 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.108-1681dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133063289 | ||||||
chr5:133063325 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.108-1655C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063325 | |||||||
chr5:133063346 | T | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.108-1634T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063346 | |||||||
chr5:133063416 | G | A | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-1564G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063416 | |||||||
chr5:133063471 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.108-1509C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063471 | |||||||
chr5:133063502 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-1478C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063502 | |||||||
chr5:133063513 | C | T | 3 | a0001c0002t0002g0052 a0001c0002t0002g0071 a0001c0002t0030g0028 |
3 | HG00140.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.108-1467C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063513 | |||||||
chr5:133063575 | C | T | 66 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.108-1405C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063575 | |||||||
chr5:133063641 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.108-1339G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063641 | |||||||
chr5:133063651 | T | G | 6 | a0001c0001t0036g0015 a0001c0004t0011g0011 a0001c0004t0011g0013 others(3): Show |
6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-1329T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063651 | |||||||
chr5:133063652 | C | G | 1 | a0001c0002t0002g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.108-1328C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063652 | |||||||
chr5:133063687 | C | T | 3 | a0001c0001t0001g0247 a0001c0001t0001g0313 a0001c0011t0001g0196 |
3 | HG01884.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.108-1293C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063687 | |||||||
chr5:133063728 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.108-1252C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063728 | |||||||
chr5:133063731 | C | A | 1 | a0001c0002t0002g0071 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.108-1249C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063731 | |||||||
chr5:133063887 | G | C | 1 | a0005c0009t0001g0291 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.108-1093G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063887 | |||||||
chr5:133064009 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.108-971G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064009 | |||||||
chr5:133064041 | C | T | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.108-939C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064041 | |||||||
chr5:133064067 | A | G | 60 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.108-913A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064067 | |||||||
chr5:133064084 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.108-896T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064084 | |||||||
chr5:133064234 | G | A | 2 | a0001c0001t0004g0076 a0001c0001t0005g0021 |
2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.108-746G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064234 | |||||||
chr5:133064244 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108-736G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064244 | |||||||
chr5:133064252 | C | T | 90 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(87): Show |
92 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.108-728C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064252 | |||||||
chr5:133064340 | T | G | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-640T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064340 | |||||||
chr5:133064367 | G | A | 3 | a0001c0002t0002g0052 a0001c0002t0002g0071 a0001c0002t0030g0028 |
3 | HG00140.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.108-613G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064367 | |||||||
chr5:133064503 | G | GA | 23 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(20): Show |
23 | HG01496.hp1 HG01516.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.108-464dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133064503 | ||||||
chr5:133064503 | GA | G | 6 | a0001c0001t0001g0085 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG01106.hp2 HG01258.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-464delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133064503 | ||||||
chr5:133064585 | C | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.108-395C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064585 | |||||||
chr5:133064663 | ATTATTTT | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0184 |
3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.108-316_108-310del others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064663 | |||||||
chr5:133064672 | T | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0184 |
3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.108-308T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064672 | |||||||
chr5:133064863 | A | G | 2 | a0001c0002t0002g0051 a0001c0002t0005g0070 |
2 | HG00621.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.108-117A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064863 | |||||||
chr5:133065168 | T | A | 1 | a0001c0001t0005g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+131T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065168 | |||||||
chr5:133065179 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18979.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.165+142C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065179 | |||||||
chr5:133065461 | C | G | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+424C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065461 | |||||||
chr5:133065816 | C | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0286 |
2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.165+779C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065816 | |||||||
chr5:133065964 | G | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.165+927G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065964 | |||||||
chr5:133066038 | G | A | 149 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(146): Show |
152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.165+1001G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066038 | |||||||
chr5:133066174 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.165+1137G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066174 | |||||||
chr5:133066232 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.166-1185C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066232 | |||||||
chr5:133066290 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.166-1127C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066290 | |||||||
chr5:133066409 | T | C | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.166-1008T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066409 | |||||||
chr5:133066610 | C | T | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.166-807C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066610 | |||||||
chr5:133066675 | AT | A | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.166-732delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133066675 | ||||||
chr5:133066736 | C | CT | 7 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0115 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-664dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133066736 | ||||||
chr5:133066736 | CT | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0083 others(18): Show |
22 | HG01169.hp2 HG01243.hp2 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.166-664delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133066736 | ||||||
chr5:133066736 | CTT | C | 62 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(59): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.166-665_166-664del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133066736 | ||||||
chr5:133066742 | T | C | 1 | a0001c0002t0002g0050 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.166-675T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066742 | |||||||
chr5:133066743 | T | C | 61 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(58): Show |
63 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.166-674T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066743 | |||||||
chr5:133066770 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.166-647A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066770 | |||||||
chr5:133066807 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(53): Show |
57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.166-610C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066807 | |||||||
chr5:133066808 | A | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-609A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066808 | |||||||
chr5:133066835 | C | T | 1 | a0001c0002t0035g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.166-582C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066835 | |||||||
chr5:133067046 | T | C | 66 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.166-371T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067046 | |||||||
chr5:133067079 | T | C | 4 | a0001c0001t0010g0281 a0001c0001t0010g0282 a0001c0001t0010g0283 others(1): Show |
4 | HG00280.hp1 NA18940.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-338T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067079 | |||||||
chr5:133067147 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.166-270T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067147 | |||||||
chr5:133067238 | C | T | 1 | a0001c0002t0002g0002 | 2 | HG02129.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.166-179C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067238 | |||||||
chr5:133067261 | A | G | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-156A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067261 | |||||||
chr5:133067293 | A | G | 1 | a0001c0001t0024g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.166-124A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067293 | |||||||
chr5:133067363 | A | T | 1 | a0001c0001t0014g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.166-54A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067363 | |||||||
chr5:133067365 | T | TA | 63 | a0001c0001t0001g0216 a0001c0001t0004g0076 a0001c0001t0005g0021 others(60): Show |
65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.166-42dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133067365 | ||||||
chr5:133067365 | T | TAA | 8 | a0001c0002t0002g0030 a0001c0002t0004g0033 a0001c0002t0004g0056 others(5): Show |
8 | HG00642.hp2 HG01516.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-43_166-42dupAA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133067365 | ||||||
chr5:133067617 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0205 a0001c0001t0001g0278 others(11): Show |
15 | HG00544.hp2 HG01192.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.306+60A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067617 | |||||||
chr5:133067649 | C | T | 149 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(146): Show |
152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.306+92C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067649 | |||||||
chr5:133067667 | T | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(145): Show |
151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.306+110T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067667 | |||||||
chr5:133067710 | T | G | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.306+153T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067710 | |||||||
chr5:133067741 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(150): Show |
156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.306+184A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067741 | |||||||
chr5:133067760 | T | C | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+203T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067760 | |||||||
chr5:133067892 | G | GT | 17 | a0001c0001t0001g0111 a0001c0001t0001g0183 a0001c0001t0001g0189 others(14): Show |
17 | HG00642.hp1 HG01175.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.306+353dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133067892 | ||||||
chr5:133067914 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.306+357A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067914 | |||||||
chr5:133068066 | G | A | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+509G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068066 | |||||||
chr5:133068135 | C | G | 186 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0080 others(183): Show |
189 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.306+578C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068135 | |||||||
chr5:133068181 | C | T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+624C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068181 | |||||||
chr5:133068195 | A | G | 63 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(60): Show |
65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.306+638A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068195 | |||||||
chr5:133068223 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(53): Show |
57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.306+666A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068223 | |||||||
chr5:133068323 | G | C | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+766G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068323 | |||||||
chr5:133068431 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.306+874A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068431 | |||||||
chr5:133068433 | G | T | 1 | a0008c0013t0001g0131 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.306+876G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068433 | |||||||
chr5:133068445 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG00408.hp1 HG02523.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.306+888C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068445 | |||||||
chr5:133068471 | A | T | 149 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(146): Show |
152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.306+914A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068471 | |||||||
chr5:133068660 | T | G | 1 | a0001c0001t0007g0192 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.306+1103T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068660 | |||||||
chr5:133068769 | TAAAG | T | 8 | a0001c0001t0008g0149 a0001c0001t0012g0017 a0001c0001t0036g0015 others(5): Show |
8 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+1216_306+1219d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133068769 | ||||||
chr5:133068784 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.306+1227G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068784 | |||||||
chr5:133068866 | C | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+1309C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068866 | |||||||
chr5:133068872 | TAA | T | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+1318_306+1319d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133068872 | ||||||
chr5:133068903 | C | G | 3 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 |
3 | NA18942.hp1 NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.306+1346C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068903 | |||||||
chr5:133069043 | C | T | 62 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(59): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.307-1331C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069043 | |||||||
chr5:133069230 | G | GTTCA | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.307-1141_307-1138d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133069230 | ||||||
chr5:133069255 | T | A | 62 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(59): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.307-1119T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069255 | |||||||
chr5:133069255 | T | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.307-1119T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069255 | |||||||
chr5:133069256 | T | A | 2 | a0001c0002t0005g0031 a0007c0008t0029g0018 |
2 | HG01516.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.307-1118T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069256 | |||||||
chr5:133069441 | G | C | 20 | a0001c0001t0001g0085 a0001c0001t0001g0159 a0001c0001t0001g0160 others(17): Show |
20 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.307-933G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069441 | |||||||
chr5:133069614 | T | C | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-760T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069614 | |||||||
chr5:133069758 | A | T | 2 | a0001c0002t0004g0033 a0001c0002t0006g0032 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.307-616A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069758 | |||||||
chr5:133069945 | C | G | 74 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(71): Show |
76 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.307-429C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069945 | |||||||
chr5:133070052 | C | T | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.307-322C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133070052 | |||||||
chr5:133070193 | A | T | 45 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(42): Show |
47 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.307-181A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133070193 | |||||||
chr5:133070239 | C | CT | 65 | a0001c0001t0001g0185 a0001c0001t0001g0280 a0001c0001t0004g0076 others(62): Show |
67 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.307-122dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133070239 | ||||||
chr5:133070271 | A | G | 1 | a0001c0002t0002g0002 | 2 | HG02129.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.307-103A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133070271 | |||||||
chr5:133070355 | C | T | 2 | a0001c0001t0004g0076 a0001c0001t0005g0021 |
2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.307-19C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133070355 | |||||||
chr5:133070598 | T | C | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.429+102T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133070598 | |||||||
chr5:133070624 | G | A | 1 | a0001c0002t0002g0035 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.429+128G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133070624 | |||||||
chr5:133070730 | C | T | 4 | a0001c0001t0001g0162 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): Show |
4 | HG02486.hp1 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+234C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133070730 | |||||||
chr5:133070906 | GA | G | 63 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(60): Show |
65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.429+420delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133070906 | ||||||
chr5:133071067 | C | T | 1 | a0001c0002t0004g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.429+571C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071067 | |||||||
chr5:133071284 | C | CA | 73 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0160 others(70): Show |
74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.429+815dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | ||||||
chr5:133071284 | C | CAA | 7 | a0001c0001t0001g0079 a0001c0001t0001g0134 a0001c0001t0001g0148 others(4): Show |
7 | HG02027.hp2 HG02647.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+814_429+815dup others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | ||||||
chr5:133071284 | CA | C | 24 | a0001c0001t0001g0086 a0001c0001t0001g0128 a0001c0001t0001g0141 others(21): Show |
24 | HG00642.hp2 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.429+815delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | ||||||
chr5:133071284 | CAA | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0083 others(66): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.429+814_429+815del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | ||||||
chr5:133071284 | CAAA | C | 36 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(33): Show |
36 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.429+813_429+815del others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | ||||||
chr5:133071366 | C | T | 78 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(75): Show |
80 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.429+870C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071366 | |||||||
chr5:133071441 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.429+945C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071441 | |||||||
chr5:133071446 | TCAAAAAA others(6): Show |
T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.429+959_429+971del others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071446 | ||||||
chr5:133071515 | A | G | 1 | a0001c0002t0005g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.429+1019A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071515 | |||||||
chr5:133071601 | C | T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG01167.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+1105C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071601 | |||||||
chr5:133071605 | C | T | 11 | a0001c0001t0001g0134 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
11 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+1109C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071605 | |||||||
chr5:133071635 | A | T | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.429+1139A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071635 | |||||||
chr5:133071716 | C | T | 1 | a0001c0001t0001g0355 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.429+1220C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071716 | |||||||
chr5:133071996 | T | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0077 others(58): Show |
63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.430-1234T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071996 | |||||||
chr5:133072004 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(53): Show |
57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.430-1226G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072004 | |||||||
chr5:133072264 | G | A | 5 | a0001c0001t0001g0257 a0001c0001t0001g0261 a0001c0001t0001g0266 others(2): Show |
5 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-966G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072264 | |||||||
chr5:133072335 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.430-895A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072335 | |||||||
chr5:133072377 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.430-853G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072377 | |||||||
chr5:133072389 | G | GTTGTTTT others(8): Show |
3 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0014 |
3 | HG02055.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.430-831_430-830ins others(15): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072389 | ||||||
chr5:133072392 | G | GT | 62 | a0001c0001t0001g0085 a0001c0001t0001g0159 a0001c0001t0001g0160 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.430-815dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | ||||||
chr5:133072392 | G | GTT | 15 | a0001c0001t0001g0167 a0001c0001t0001g0179 a0001c0001t0001g0181 others(12): Show |
15 | HG01167.hp2 HG01346.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-816_430-815dup others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | ||||||
chr5:133072392 | G | GTTT | 9 | a0001c0002t0002g0030 a0001c0002t0004g0003 a0001c0002t0004g0057 others(6): Show |
9 | HG00639.hp2 HG01169.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.430-817_430-815dup others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | ||||||
chr5:133072392 | G | GTTTT | 29 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(26): Show |
31 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.430-818_430-815dup others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | ||||||
chr5:133072392 | G | GTTTTT | 15 | a0001c0001t0001g0148 a0001c0002t0002g0034 a0001c0002t0002g0035 others(12): Show |
15 | HG01993.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-819_430-815dup others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | ||||||
chr5:133072392 | G | T | 1 | a0001c0002t0002g0068 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.430-838G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072392 | |||||||
chr5:133072392 | GT | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0079 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.430-815delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | ||||||
chr5:133072392 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430-825_430-815del others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | ||||||
chr5:133072393 | T | TTTTTTTG others(7): Show |
4 | a0001c0004t0011g0011 a0001c0004t0011g0013 a0001c0004t0012g0012 others(1): Show |
4 | HG02922.hp1 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-831_430-830ins others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072393 | ||||||
chr5:133072409 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.430-821T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072409 | |||||||
chr5:133072562 | A | AT | 9 | a0001c0001t0001g0202 a0001c0001t0001g0223 a0001c0001t0001g0250 others(6): Show |
9 | HG01175.hp2 HG01261.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.430-652dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072562 | ||||||
chr5:133072562 | AT | A | 10 | a0001c0001t0001g0148 a0001c0001t0001g0194 a0001c0001t0025g0344 others(7): Show |
10 | HG00438.hp2 HG01069.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-652delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072562 | ||||||
chr5:133072565 | T | TA | 2 | a0001c0001t0001g0004 a0001c0001t0001g0184 |
3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.430-665_430-664ins others(1): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072565 | |||||||
chr5:133072566 | T | A | 54 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0083 others(51): Show |
54 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.430-664T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072566 | |||||||
chr5:133072673 | C | T | 1 | a0001c0002t0035g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.430-557C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072673 | |||||||
chr5:133072760 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.430-470A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072760 | |||||||
chr5:133072777 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.430-453C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072777 | |||||||
chr5:133072869 | T | G | 1 | a0001c0001t0001g0330 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.430-361T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072869 | |||||||
chr5:133072891 | T | C | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.430-339T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072891 | |||||||
chr5:133072939 | T | C | 152 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(149): Show |
155 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.430-291T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072939 | |||||||
chr5:133073052 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-178C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133073052 | |||||||
chr5:133073341 | C | T | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.529+12C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073341 | |||||||
chr5:133073382 | A | G | 63 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(60): Show |
65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.529+53A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073382 | |||||||
chr5:133073389 | A | G | 2 | a0001c0001t0014g0150 a0001c0001t0014g0151 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.529+60A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073389 | |||||||
chr5:133073564 | G | T | 1 | a0001c0001t0022g0106 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.529+235G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073564 | |||||||
chr5:133073649 | G | C | 2 | a0001c0001t0001g0326 a0001c0001t0001g0331 |
2 | HG00544.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.529+320G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073649 | |||||||
chr5:133073674 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.530-319A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073674 | |||||||
chr5:133073684 | G | A | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.530-309G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073684 | |||||||
chr5:133073724 | A | G | 2 | a0001c0001t0014g0150 a0001c0001t0014g0151 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.530-269A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073724 | |||||||
chr5:133073844 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.530-149A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073844 | |||||||
chr5:133073902 | A | C | 3 | a0001c0001t0001g0226 a0001c0001t0001g0264 a0001c0001t0001g0315 |
3 | NA18998.hp2 NA19006.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.530-91A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073902 | |||||||
chr5:133073958 | C | T | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.530-35C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073958 | |||||||
chr5:133074175 | T | G | 60 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.663+49T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074175 | |||||||
chr5:133074184 | G | A | 1 | a0001c0001t0012g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.663+58G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074184 | |||||||
chr5:133074212 | A | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.663+86A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074212 | |||||||
chr5:133074232 | AC | A | 3 | a0001c0002t0013g0026 a0001c0002t0013g0042 a0001c0002t0013g0058 |
3 | HG00639.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.663+108delC | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 133074232 | ||||||
chr5:133074233 | C | T | 1 | a0001c0002t0002g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.663+107C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074233 | |||||||
chr5:133074283 | CT | C | 72 | a0001c0001t0001g0119 a0001c0001t0001g0289 a0001c0001t0004g0076 others(69): Show |
74 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.663+169delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 133074283 | ||||||
chr5:133074292 | T | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+166T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074292 | |||||||
chr5:133074307 | T | G | 60 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.663+181T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074307 | |||||||
chr5:133074341 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0204 |
2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.663+215C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074341 | |||||||
chr5:133074361 | C | T | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.663+235C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074361 | |||||||
chr5:133074422 | G | T | 2 | a0001c0001t0001g0114 a0001c0001t0023g0113 |
2 | NA18989.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.663+296G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074422 | |||||||
chr5:133074439 | C | T | 2 | a0003c0005t0001g0169 a0003c0005t0001g0174 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.663+313C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074439 | |||||||
chr5:133074581 | G | A | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+455G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074581 | |||||||
chr5:133074812 | T | C | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.663+686T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074812 | |||||||
chr5:133074822 | T | C | 3 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 |
3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.663+696T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074822 | |||||||
chr5:133075044 | G | C | 1 | a0001c0001t0009g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.663+918G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075044 | |||||||
chr5:133075133 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.663+1007G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075133 | |||||||
chr5:133075139 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.663+1013T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075139 | |||||||
chr5:133075376 | T | G | 2 | a0001c0001t0036g0015 a0001c0015t0012g0016 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.663+1250T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075376 | |||||||
chr5:133075430 | C | T | 1 | a0001c0001t0012g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.664-1224C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075430 | |||||||
chr5:133075644 | A | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-1010A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075644 | |||||||
chr5:133075739 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(150): Show |
156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.664-915G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075739 | |||||||
chr5:133075769 | A | G | 1 | a0002c0003t0003g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.664-885A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075769 | |||||||
chr5:133075848 | TAAAG | T | 51 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(48): Show |
51 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.664-802_664-799del others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 133075848 | ||||||
chr5:133075884 | A | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-770A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075884 | |||||||
chr5:133075994 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0184 |
3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.664-660G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075994 | |||||||
chr5:133075997 | G | C | 1 | a0001c0001t0001g0273 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.664-657G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075997 | |||||||
chr5:133076077 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0272 |
2 | NA18964.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.664-577A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133076077 | |||||||
chr5:133076392 | A | T | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.664-262A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133076392 | |||||||
chr5:133076607 | A | G | 60 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.664-47A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133076607 | |||||||
chr5:133076650 | T | A | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.664-4T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133076650 | |||||||
chr5:133076988 | C | T | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+90C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133076988 | |||||||
chr5:133077156 | C | T | 62 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(59): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.908+258C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077156 | |||||||
chr5:133077327 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.908+429C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077327 | |||||||
chr5:133077358 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0341 |
2 | HG02040.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.908+460C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077358 | |||||||
chr5:133077360 | C | T | 4 | a0002c0003t0001g0154 a0002c0003t0001g0182 a0002c0003t0003g0155 others(1): Show |
4 | HG01074.hp2 HG01175.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+462C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077360 | |||||||
chr5:133077394 | C | T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.908+496C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077394 | |||||||
chr5:133077471 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.908+573C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077471 | |||||||
chr5:133077562 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.908+664C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077562 | |||||||
chr5:133077628 | C | T | 1 | a0001c0002t0028g0063 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.908+730C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077628 | |||||||
chr5:133077629 | G | A | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.908+731G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077629 | |||||||
chr5:133077641 | A | C | 1 | a0001c0001t0001g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.908+743A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077641 | |||||||
chr5:133077646 | CT | C | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.908+749delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077646 | |||||||
chr5:133077754 | T | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+856T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077754 | |||||||
chr5:133077884 | T | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA18939.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.908+986T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077884 | |||||||
chr5:133077960 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.908+1062G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077960 | |||||||
chr5:133078039 | G | C | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1141G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078039 | |||||||
chr5:133078061 | G | A | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+1163G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078061 | |||||||
chr5:133078092 | G | A | 1 | a0001c0002t0005g0022 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.908+1194G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078092 | |||||||
chr5:133078286 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1388C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078286 | |||||||
chr5:133078346 | A | G | 1 | a0001c0001t0001g0303 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.908+1448A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078346 | |||||||
chr5:133078462 | C | T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.908+1564C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078462 | |||||||
chr5:133078492 | G | C | 1 | a0001c0002t0002g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.908+1594G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078492 | |||||||
chr5:133078508 | G | A | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1610G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078508 | |||||||
chr5:133078634 | CCAAAAAA | C | 6 | a0001c0001t0036g0015 a0001c0004t0011g0011 a0001c0004t0011g0013 others(3): Show |
6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1737_908+1743d others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078634 | |||||||
chr5:133078635 | C | CA | 84 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(81): Show |
86 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.908+1759dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | ||||||
chr5:133078635 | CA | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0109 others(3): Show |
6 | HG01074.hp2 HG01515.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1759delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | ||||||
chr5:133078635 | CAA | C | 15 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(12): Show |
15 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.908+1758_908+1759d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | ||||||
chr5:133078635 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0219 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.908+1750_908+1759d others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | ||||||
chr5:133078635 | CAAAAAAA others(5): Show |
C | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.908+1748_908+1759d others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | ||||||
chr5:133078668 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.908+1770A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078668 | |||||||
chr5:133078686 | C | T | 1 | a0001c0002t0006g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.908+1788C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078686 | |||||||
chr5:133078696 | A | T | 3 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 |
3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.908+1798A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078696 | |||||||
chr5:133078732 | ATTG | A | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1843_908+1845d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078732 | ||||||
chr5:133078739 | T | C | 1 | a0001c0001t0012g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.908+1841T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078739 | |||||||
chr5:133078841 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.908+1943C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078841 | |||||||
chr5:133078880 | C | T | 1 | a0001c0002t0006g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.908+1982C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078880 | |||||||
chr5:133079090 | T | A | 4 | a0001c0002t0004g0003 a0001c0002t0004g0074 a0001c0002t0004g0075 others(1): Show |
4 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+2192T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079090 | |||||||
chr5:133079233 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0142 a0001c0001t0001g0146 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+2335G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079233 | |||||||
chr5:133079442 | G | C | 1 | a0001c0002t0002g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.908+2544G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079442 | |||||||
chr5:133079586 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.908+2688A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079586 | |||||||
chr5:133079637 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.908+2739A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079637 | |||||||
chr5:133079730 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.908+2832C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079730 | |||||||
chr5:133079754 | G | A | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+2856G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079754 | |||||||
chr5:133079810 | C | T | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.908+2912C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079810 | |||||||
chr5:133079877 | A | G | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.908+2979A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079877 | |||||||
chr5:133080188 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+3290C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080188 | |||||||
chr5:133080189 | G | A | 4 | a0001c0002t0002g0035 a0001c0002t0002g0036 a0001c0002t0002g0037 others(1): Show |
4 | NA18960.hp1 NA18994.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+3291G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080189 | |||||||
chr5:133080204 | A | G | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.908+3306A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080204 | |||||||
chr5:133080417 | C | CA | 97 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0083 others(94): Show |
98 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.908+3543dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133080417 | ||||||
chr5:133080417 | C | CAA | 26 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0092 others(23): Show |
26 | HG00438.hp1 HG00609.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.908+3542_908+3543d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133080417 | ||||||
chr5:133080417 | CAA | C | 54 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0023 others(51): Show |
56 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.908+3542_908+3543d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133080417 | ||||||
chr5:133080437 | A | G | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.908+3539A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080437 | |||||||
chr5:133080442 | C | A | 4 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0014g0150 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+3544C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080442 | |||||||
chr5:133080499 | C | T | 1 | a0001c0002t0002g0038 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.908+3601C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080499 | |||||||
chr5:133080500 | A | G | 7 | a0001c0002t0002g0023 a0001c0002t0002g0038 a0001c0002t0002g0039 others(4): Show |
8 | HG00323.hp2 HG01255.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.908+3602A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080500 | |||||||
chr5:133080569 | G | C | 4 | a0001c0002t0004g0003 a0001c0002t0004g0074 a0001c0002t0004g0075 others(1): Show |
4 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+3671G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080569 | |||||||
chr5:133080591 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.908+3693A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080591 | |||||||
chr5:133080680 | A | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18974.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.908+3782A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080680 | |||||||
chr5:133080680 | AT | A | 6 | a0001c0001t0001g0209 a0001c0001t0001g0256 a0001c0001t0001g0268 others(3): Show |
6 | NA18964.hp1 NA18989.hp2 NA19074.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+3791delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133080680 | ||||||
chr5:133080682 | T | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0262 others(9): Show |
12 | HG01243.hp2 HG02129.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.908+3784T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080682 | |||||||
chr5:133080779 | A | G | 4 | a0001c0004t0011g0011 a0001c0004t0011g0013 a0001c0004t0011g0014 others(1): Show |
4 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+3881A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080779 | |||||||
chr5:133080785 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.908+3887A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080785 | |||||||
chr5:133080860 | T | C | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+3962T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080860 | |||||||
chr5:133081094 | C | G | 1 | a0001c0001t0001g0265 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.908+4196C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081094 | |||||||
chr5:133081130 | C | T | 50 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(47): Show |
50 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.908+4232C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081130 | |||||||
chr5:133081355 | T | C | 4 | a0001c0001t0001g0089 a0001c0001t0001g0101 a0001c0001t0001g0107 others(1): Show |
4 | NA18944.hp2 NA18970.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+4457T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081355 | |||||||
chr5:133081492 | G | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.908+4594G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081492 | |||||||
chr5:133081656 | C | T | 4 | a0002c0003t0001g0154 a0002c0003t0001g0182 a0002c0003t0003g0155 others(1): Show |
4 | HG01074.hp2 HG01175.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+4758C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081656 | |||||||
chr5:133081830 | G | A | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.908+4932G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081830 | |||||||
chr5:133081882 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.909-4900T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081882 | |||||||
chr5:133081978 | T | C | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-4804T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081978 | |||||||
chr5:133082034 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.909-4748A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082034 | |||||||
chr5:133082150 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(75): Show |
79 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.909-4632G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082150 | |||||||
chr5:133082232 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.909-4550C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082232 | |||||||
chr5:133082303 | A | T | 4 | a0001c0002t0004g0056 a0001c0002t0004g0057 a0001c0002t0006g0054 others(1): Show |
4 | HG00642.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-4479A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082303 | |||||||
chr5:133082344 | G | A | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.909-4438G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082344 | |||||||
chr5:133082388 | C | G | 66 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.909-4394C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082388 | |||||||
chr5:133082559 | G | A | 183 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(180): Show |
186 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.909-4223G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082559 | |||||||
chr5:133082627 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.909-4155G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082627 | |||||||
chr5:133082880 | A | G | 66 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.909-3902A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082880 | |||||||
chr5:133083062 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.909-3720G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083062 | |||||||
chr5:133083121 | C | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.909-3661C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083121 | |||||||
chr5:133083121 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.909-3661C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083121 | |||||||
chr5:133083144 | C | CA | 23 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0001c0001t0001g0115 others(20): Show |
23 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.909-3620dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133083144 | ||||||
chr5:133083144 | C | CAA | 6 | a0001c0004t0011g0011 a0001c0004t0011g0013 a0001c0004t0011g0014 others(3): Show |
6 | HG01175.hp1 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.909-3621_909-3620d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133083144 | ||||||
chr5:133083163 | T | A | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-3619T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083163 | |||||||
chr5:133083165 | A | T | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-3617A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083165 | |||||||
chr5:133083166 | C | A | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-3616C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083166 | |||||||
chr5:133083180 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.909-3602C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083180 | |||||||
chr5:133083243 | C | T | 1 | a0001c0001t0014g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.909-3539C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083243 | |||||||
chr5:133083282 | A | T | 67 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(64): Show |
69 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.909-3500A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083282 | |||||||
chr5:133083421 | A | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0180 a0001c0001t0003g0176 |
3 | HG01891.hp1 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.909-3361A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083421 | |||||||
chr5:133083597 | G | A | 1 | a0001c0001t0015g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.909-3185G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083597 | |||||||
chr5:133083624 | G | C | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.909-3158G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083624 | |||||||
chr5:133083691 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.909-3091C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083691 | |||||||
chr5:133083733 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.909-3049C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083733 | |||||||
chr5:133083907 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.909-2875C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083907 | |||||||
chr5:133084033 | A | G | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.909-2749A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084033 | |||||||
chr5:133084074 | A | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2708A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084074 | |||||||
chr5:133084122 | G | A | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.909-2660G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084122 | |||||||
chr5:133084137 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.909-2645T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084137 | |||||||
chr5:133084257 | T | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2525T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084257 | |||||||
chr5:133084365 | C | T | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.909-2417C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084365 | |||||||
chr5:133084590 | C | T | 10 | a0001c0001t0001g0085 a0001c0001t0001g0159 a0001c0001t0001g0163 others(7): Show |
10 | HG01106.hp2 HG01258.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-2192C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084590 | |||||||
chr5:133084697 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2085C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084697 | |||||||
chr5:133084716 | C | T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.909-2066C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084716 | |||||||
chr5:133084771 | A | G | 3 | a0001c0002t0002g0038 a0001c0002t0018g0001 a0001c0002t0032g0029 |
4 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.909-2011A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084771 | |||||||
chr5:133084777 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.909-2005C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084777 | |||||||
chr5:133084800 | A | G | 3 | a0001c0002t0002g0052 a0001c0002t0002g0071 a0001c0002t0030g0028 |
3 | HG00140.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.909-1982A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084800 | |||||||
chr5:133084811 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-1971C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084811 | |||||||
chr5:133084956 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.909-1826C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084956 | |||||||
chr5:133085134 | TA | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-1639delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085134 | ||||||
chr5:133085234 | A | C | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-1548A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085234 | |||||||
chr5:133085410 | TGGAAGGT others(5): Show |
T | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-1371_909-1360d others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085410 | |||||||
chr5:133085489 | T | TAAAAAAA others(5): Show |
3 | a0001c0001t0001g0086 a0001c0001t0001g0142 a0001c0001t0001g0147 |
3 | HG02630.hp2 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.909-1291_909-1280d others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(6): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0146 |
3 | HG00558.hp1 NA18945.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.909-1292_909-1280d others(15): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(7): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0089 a0001c0001t0001g0101 others(4): Show |
8 | HG03225.hp1 HG03486.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(16): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(8): Show |
51 | a0001c0001t0004g0076 a0001c0001t0009g0350 a0001c0001t0009g0351 others(48): Show |
53 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(17): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(9): Show |
13 | a0001c0001t0005g0021 a0001c0001t0012g0017 a0001c0001t0036g0015 others(10): Show |
13 | HG01358.hp1 HG01433.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(18): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(11): Show |
5 | a0001c0001t0001g0122 a0001c0001t0023g0113 a0001c0004t0011g0013 others(2): Show |
5 | HG01516.hp1 HG02055.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(20): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(12): Show |
1 | a0001c0004t0011g0011 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(21): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(23): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.909-1280_909-1279i others(25): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(20): Show |
3 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0152 |
3 | HG02572.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(29): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(21): Show |
4 | a0001c0001t0001g0130 a0001c0001t0014g0150 a0001c0001t0014g0151 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(30): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(22): Show |
2 | a0001c0001t0001g0133 a0001c0001t0008g0149 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(31): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(23): Show |
2 | a0001c0001t0001g0141 a0001c0007t0001g0144 |
2 | HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(32): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(24): Show |
2 | a0001c0001t0001g0137 a0001c0001t0001g0140 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(33): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(25): Show |
9 | a0001c0001t0001g0078 a0001c0001t0001g0100 a0001c0001t0001g0127 others(6): Show |
9 | HG00609.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(34): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(26): Show |
12 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(9): Show |
12 | HG00438.hp1 HG02074.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(35): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(27): Show |
6 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0120 others(3): Show |
6 | HG02109.hp1 HG02300.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(36): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(28): Show |
5 | a0001c0001t0001g0087 a0001c0001t0001g0094 a0001c0001t0001g0096 others(2): Show |
5 | HG02080.hp2 HG02615.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(37): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(29): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0111 |
2 | NA18972.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(38): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(30): Show |
2 | a0001c0001t0001g0118 a0001c0001t0001g0143 |
2 | HG02559.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(39): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(31): Show |
3 | a0001c0001t0001g0135 a0001c0001t0022g0106 a0009c0010t0003g0138 |
3 | HG03540.hp1 NA18993.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(40): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(32): Show |
2 | a0001c0001t0001g0098 a0001c0001t0001g0123 |
2 | NA18939.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(41): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(34): Show |
1 | a0001c0001t0001g0119 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(43): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(35): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0121 |
2 | NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(44): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(36): Show |
1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(45): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(37): Show |
1 | a0001c0001t0001g0108 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(46): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TAAAAAAA others(51): Show |
1 | a0001c0001t0001g0126 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.909-1280_909-1279i others(60): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | ||||||
chr5:133085489 | T | TTAAAAAA others(19): Show |
3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.909-1293_909-1292i others(28): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085489 | |||||||
chr5:133085503 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.909-1279T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085503 | |||||||
chr5:133085511 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.909-1271T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085511 | |||||||
chr5:133085519 | C | G | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG01167.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.909-1263C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085519 | |||||||
chr5:133085637 | G | A | 1 | a0001c0015t0012g0016 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.909-1145G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085637 | |||||||
chr5:133085689 | A | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG01243.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.909-1093A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085689 | |||||||
chr5:133085737 | GCAGGGAG others(18): Show |
G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(75): Show |
79 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.909-1013_909-989de others(26): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085737 | ||||||
chr5:133085857 | C | T | 60 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.909-925C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085857 | |||||||
chr5:133085980 | G | A | 1 | a0001c0002t0002g0062 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.909-802G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085980 | |||||||
chr5:133085987 | A | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-795A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085987 | |||||||
chr5:133086185 | A | G | 1 | a0001c0002t0002g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.909-597A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086185 | |||||||
chr5:133086219 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.909-563A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086219 | |||||||
chr5:133086267 | CTCT | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(83): Show |
87 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.909-506_909-504del others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133086267 | ||||||
chr5:133086298 | G | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(83): Show |
87 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.909-484G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086298 | |||||||
chr5:133086299 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.909-483C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086299 | |||||||
chr5:133086437 | G | A | 10 | a0001c0001t0001g0085 a0001c0001t0001g0159 a0001c0001t0001g0163 others(7): Show |
10 | HG01106.hp2 HG01258.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-345G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086437 | |||||||
chr5:133086567 | C | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-215C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086567 | |||||||
chr5:133086580 | G | T | 2 | a0001c0001t0014g0150 a0001c0001t0014g0151 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.909-202G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086580 | |||||||
chr5:133086760 | T | G | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-22T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086760 | |||||||
chr5:133086761 | G | T | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-21G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086761 | |||||||
chr5:133086889 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.985+31G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133086889 | |||||||
chr5:133086998 | A | T | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.985+140A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133086998 | |||||||
chr5:133087025 | A | T | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.985+167A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087025 | |||||||
chr5:133087133 | C | CT | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01167.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.985+279dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 133087133 | ||||||
chr5:133087151 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.985+293G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087151 | |||||||
chr5:133087194 | G | T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.985+336G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087194 | |||||||
chr5:133087309 | T | C | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.985+451T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087309 | |||||||
chr5:133087397 | C | CT | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.985+541dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 133087397 | ||||||
chr5:133087575 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.985+717C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087575 | |||||||
chr5:133087587 | C | G | 6 | a0001c0001t0036g0015 a0001c0004t0011g0011 a0001c0004t0011g0013 others(3): Show |
6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.985+729C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087587 | |||||||
chr5:133087633 | T | A | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.986-771T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087633 | |||||||
chr5:133087634 | A | T | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.986-770A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087634 | |||||||
chr5:133087760 | A | C | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.986-644A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087760 | |||||||
chr5:133087772 | C | T | 13 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0221 others(10): Show |
13 | HG01192.hp2 HG01978.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.986-632C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087772 | |||||||
chr5:133087869 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.986-535C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087869 | |||||||
chr5:133088020 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.986-384C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088020 | |||||||
chr5:133088063 | C | G | 1 | a0001c0001t0001g0224 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.986-341C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088063 | |||||||
chr5:133088072 | T | C | 58 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(55): Show |
58 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.986-332T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088072 | |||||||
chr5:133088109 | G | A | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.986-295G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088109 | |||||||
chr5:133088277 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(84): Show |
88 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.986-127G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088277 | |||||||
chr5:133088354 | T | C | 3 | a0001c0001t0001g0168 a0001c0001t0003g0170 a0001c0001t0003g0175 |
3 | HG01099.hp1 HG01346.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.986-50T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088354 | |||||||
chr5:133088783 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1137+228A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 9/18 | chr5 | 133088783 | |||||||
chr5:133089028 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0337 |
2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1138-27C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 9/18 | chr5 | 133089028 | |||||||
chr5:133089051 | C | T | 50 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(47): Show |
50 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
splice_region_variant&intron_variant | LOW | c.1138-4C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 9/18 | chr5 | 133089051 | |||||||
chr5:133089259 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1244+98A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089259 | |||||||
chr5:133089271 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244+110T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089271 | |||||||
chr5:133089289 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1244+128A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089289 | |||||||
chr5:133089357 | A | G | 186 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0080 others(183): Show |
189 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.1244+196A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089357 | |||||||
chr5:133089477 | G | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(83): Show |
87 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1245-85G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089477 | |||||||
chr5:133089723 | G | GA | 79 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(76): Show |
80 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1378+42dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133089723 | ||||||
chr5:133089773 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(83): Show |
87 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1378+78A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089773 | |||||||
chr5:133089865 | A | C | 14 | a0001c0001t0001g0087 a0001c0001t0001g0094 a0001c0001t0001g0095 others(11): Show |
14 | HG00558.hp1 HG02055.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1378+170A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089865 | |||||||
chr5:133089866 | A | T | 1 | a0001c0001t0001g0251 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1378+171A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089866 | |||||||
chr5:133089907 | C | T | 2 | a0001c0001t0001g0326 a0001c0001t0001g0331 |
2 | HG00544.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1378+212C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089907 | |||||||
chr5:133089948 | A | C | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1378+253A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089948 | |||||||
chr5:133090012 | T | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378+317T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090012 | |||||||
chr5:133090112 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1378+417T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090112 | |||||||
chr5:133090182 | C | G | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1378+487C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090182 | |||||||
chr5:133090219 | G | A | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378+524G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090219 | |||||||
chr5:133090234 | G | C | 1 | a0001c0002t0027g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1378+539G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090234 | |||||||
chr5:133090235 | G | T | 4 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0014g0150 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+540G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090235 | |||||||
chr5:133090261 | C | T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1378+566C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090261 | |||||||
chr5:133090300 | G | A | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+605G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090300 | |||||||
chr5:133090305 | C | T | 17 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0132 others(14): Show |
17 | HG01243.hp2 HG01496.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1378+610C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090305 | |||||||
chr5:133090406 | A | C | 66 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1378+711A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090406 | |||||||
chr5:133090430 | C | CA | 77 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0079 others(74): Show |
79 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1379-738dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | ||||||
chr5:133090430 | C | CAA | 27 | a0001c0001t0001g0088 a0001c0001t0001g0122 a0001c0001t0001g0130 others(24): Show |
27 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1379-739_1379-738d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | ||||||
chr5:133090430 | C | CAAA | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0089 others(40): Show |
43 | HG00558.hp1 HG00609.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1379-740_1379-738d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | ||||||
chr5:133090430 | C | CAAAA | 10 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0107 others(7): Show |
10 | HG00438.hp1 HG02074.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1379-741_1379-738d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | ||||||
chr5:133090430 | CA | C | 17 | a0001c0001t0001g0190 a0001c0001t0001g0211 a0001c0001t0001g0241 others(14): Show |
17 | HG00408.hp1 HG01081.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1379-738delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | ||||||
chr5:133090430 | CAA | C | 51 | a0001c0001t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0009 others(48): Show |
53 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1379-739_1379-738d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | ||||||
chr5:133090504 | T | C | 2 | a0001c0002t0002g0052 a0001c0002t0030g0028 |
2 | HG00140.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1379-689T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090504 | |||||||
chr5:133090520 | C | T | 1 | a0001c0007t0001g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1379-673C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090520 | |||||||
chr5:133090573 | C | A | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1379-620C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090573 | |||||||
chr5:133090653 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1379-540G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090653 | |||||||
chr5:133090694 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379-499C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090694 | |||||||
chr5:133090705 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1379-488C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090705 | |||||||
chr5:133090734 | C | A | 1 | a0001c0002t0002g0034 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1379-459C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090734 | |||||||
chr5:133090808 | A | G | 17 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(14): Show |
17 | HG01496.hp1 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1379-385A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090808 | |||||||
chr5:133090959 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1379-234C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090959 | |||||||
chr5:133091159 | GTT | G | 6 | a0001c0002t0002g0034 a0001c0002t0002g0040 a0001c0002t0002g0043 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1379-33_1379-32del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133091159 | |||||||
chr5:133091598 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1560+224C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091598 | |||||||
chr5:133091696 | G | T | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1560+322G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091696 | |||||||
chr5:133091874 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1560+500A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091874 | |||||||
chr5:133091874 | AAAC | A | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1560+518_1560+520d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 133091874 | ||||||
chr5:133091895 | A | C | 1 | a0001c0002t0004g0056 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1560+521A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091895 | |||||||
chr5:133091953 | G | A | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1560+579G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091953 | |||||||
chr5:133092025 | T | C | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1560+651T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092025 | |||||||
chr5:133092042 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1561-658C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092042 | |||||||
chr5:133092057 | CAA | C | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1561-640_1561-639d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 133092057 | ||||||
chr5:133092262 | C | G | 1 | a0002c0003t0001g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1561-438C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092262 | |||||||
chr5:133092284 | G | T | 2 | a0001c0002t0004g0033 a0001c0002t0006g0032 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1561-416G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092284 | |||||||
chr5:133092503 | T | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0262 |
2 | NA18953.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1561-197T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092503 | |||||||
chr5:133092515 | A | G | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1561-185A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092515 | |||||||
chr5:133092806 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1650+25_1650+26ins others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0001g0004 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1650+25_1650+26ins others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1650+36_1650+49dup others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GT | G | 65 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0103 others(62): Show |
67 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1650+49delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GTT | G | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0077 others(109): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1650+48_1650+49del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GTTT | G | 41 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0089 others(38): Show |
41 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1650+47_1650+49del others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GTTTTTTT | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(55): Show |
60 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1650+43_1650+49del others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GTTTTTTT others(1): Show |
G | 12 | a0001c0001t0001g0134 a0001c0001t0001g0146 a0001c0001t0003g0145 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1650+42_1650+49del others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GTTTTTTT others(2): Show |
G | 14 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0135 others(11): Show |
14 | HG01496.hp1 HG01516.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1650+41_1650+49del others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0012g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1650+40_1650+49del others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0244 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1650+38_1650+49del others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092806 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0317 |
2 | HG01081.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1650+37_1650+49del others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | ||||||
chr5:133092808 | T | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0238 a0001c0001t0007g0304 |
3 | NA18945.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1650+19T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092808 | |||||||
chr5:133092809 | T | G | 3 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0001t0007g0343 |
3 | NA18993.hp1 NA19007.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1650+20T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092809 | |||||||
chr5:133092810 | T | G | 2 | a0001c0001t0001g0305 a0001c0001t0007g0192 |
2 | NA18972.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1650+21T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092810 | |||||||
chr5:133092816 | T | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1650+27T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092816 | |||||||
chr5:133092817 | T | C | 1 | a0001c0002t0002g0051 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1650+28T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092817 | |||||||
chr5:133092818 | T | C | 58 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(55): Show |
60 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1650+29T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092818 | |||||||
chr5:133092819 | T | C | 3 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0004g0075 |
3 | HG01243.hp1 HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1650+30T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092819 | |||||||
chr5:133092863 | C | A | 2 | a0001c0001t0014g0150 a0001c0001t0014g0151 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1650+74C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092863 | |||||||
chr5:133092887 | C | A | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1650+98C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092887 | |||||||
chr5:133092889 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1650+100C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092889 | |||||||
chr5:133092900 | A | C | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1650+111A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092900 | |||||||
chr5:133092956 | G | A | 1 | a0002c0003t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1650+167G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092956 | |||||||
chr5:133092985 | AT | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(68): Show |
72 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1650+212delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092985 | ||||||
chr5:133092985 | ATT | A | 59 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(56): Show |
61 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1650+211_1650+212d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092985 | ||||||
chr5:133093083 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1650+294G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093083 | |||||||
chr5:133093125 | C | T | 3 | a0001c0002t0002g0052 a0001c0002t0002g0071 a0001c0002t0030g0028 |
3 | HG00140.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1650+336C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093125 | |||||||
chr5:133093144 | G | C | 3 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 |
3 | NA18942.hp1 NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1650+355G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093144 | |||||||
chr5:133093166 | A | G | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1650+377A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093166 | |||||||
chr5:133093173 | A | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1650+384A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093173 | |||||||
chr5:133093243 | T | G | 1 | a0001c0001t0003g0145 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1650+454T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093243 | |||||||
chr5:133093255 | T | C | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1650+466T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093255 | |||||||
chr5:133093571 | G | GC | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1650+787dupC | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133093571 | ||||||
chr5:133093572 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1650+783C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093572 | |||||||
chr5:133093716 | C | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1650+927C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093716 | |||||||
chr5:133093806 | G | A | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1650+1017G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093806 | |||||||
chr5:133093860 | C | T | 43 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1650+1071C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093860 | |||||||
chr5:133093893 | G | T | 1 | a0001c0002t0002g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1650+1104G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093893 | |||||||
chr5:133093921 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1650+1132C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093921 | |||||||
chr5:133094104 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1650+1315T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094104 | |||||||
chr5:133094109 | A | G | 1 | a0001c0002t0002g0052 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1650+1320A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094109 | |||||||
chr5:133094155 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1650+1366G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094155 | |||||||
chr5:133094172 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1650+1383A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094172 | |||||||
chr5:133094304 | A | G | 1 | a0001c0001t0008g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1650+1515A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094304 | |||||||
chr5:133094462 | G | A | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1651-1636G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094462 | |||||||
chr5:133094478 | A | G | 1 | a0001c0002t0006g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1651-1620A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094478 | |||||||
chr5:133094497 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1651-1601T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094497 | |||||||
chr5:133094833 | T | C | 60 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1651-1265T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094833 | |||||||
chr5:133095000 | G | A | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1651-1098G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095000 | |||||||
chr5:133095157 | A | G | 1 | a0001c0001t0009g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1651-941A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095157 | |||||||
chr5:133095288 | C | T | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1651-810C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095288 | |||||||
chr5:133095309 | C | A | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1651-789C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095309 | |||||||
chr5:133095310 | A | G | 1 | a0001c0001t0020g0316 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1651-788A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095310 | |||||||
chr5:133095445 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1651-653A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095445 | |||||||
chr5:133095463 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(69): Show |
73 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1651-635A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095463 | |||||||
chr5:133095621 | C | T | 3 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 |
3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1651-477C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095621 | |||||||
chr5:133095693 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0305 |
2 | NA18972.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1651-405G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095693 | |||||||
chr5:133096034 | A | T | 1 | a0001c0001t0026g0354 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1651-64A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133096034 | |||||||
chr5:133096306 | A | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1803+56A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096306 | |||||||
chr5:133096383 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
6 | HG00099.hp2 HG00323.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+133G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096383 | |||||||
chr5:133096430 | C | A | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1803+180C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096430 | |||||||
chr5:133096560 | T | G | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1803+310T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096560 | |||||||
chr5:133096825 | T | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1804-336T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096825 | |||||||
chr5:133096826 | G | A | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1804-335G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096826 | |||||||
chr5:133096838 | C | T | 66 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1804-323C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096838 | |||||||
chr5:133096954 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1804-207A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096954 | |||||||
chr5:133096976 | C | G | 3 | a0001c0001t0001g0236 a0001c0001t0001g0240 a0001c0001t0021g0222 |
3 | NA18971.hp1 NA19011.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1804-185C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096976 | |||||||
chr5:133097357 | G | T | 10 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0171 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1929+71G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097357 | |||||||
chr5:133097427 | T | A | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1929+141T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097427 | |||||||
chr5:133097511 | C | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(52): Show |
56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1929+225C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097511 | |||||||
chr5:133097531 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1929+245G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097531 | |||||||
chr5:133097535 | CTTTCT | C | 8 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(5): Show |
8 | HG01167.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1929+263_1929+267d others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133097535 | ||||||
chr5:133097549 | C | CT | 59 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(56): Show |
61 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1929+279dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133097549 | ||||||
chr5:133097605 | G | A | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1929+319G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097605 | |||||||
chr5:133097631 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1929+345C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097631 | |||||||
chr5:133097815 | C | T | 4 | a0001c0002t0004g0003 a0001c0002t0004g0074 a0001c0002t0004g0075 others(1): Show |
4 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+529C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097815 | |||||||
chr5:133097891 | A | G | 6 | a0001c0001t0036g0015 a0001c0004t0011g0011 a0001c0004t0011g0013 others(3): Show |
6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+605A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097891 | |||||||
chr5:133097911 | G | GT | 9 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(6): Show |
9 | HG01106.hp2 HG01167.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1929+640dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133097911 | ||||||
chr5:133097913 | T | G | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1929+627T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097913 | |||||||
chr5:133097926 | T | A | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1929+640T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097926 | |||||||
chr5:133097929 | T | G | 1 | a0001c0002t0005g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1929+643T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097929 | |||||||
chr5:133098036 | C | T | 1 | a0001c0001t0024g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1929+750C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098036 | |||||||
chr5:133098334 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1929+1048C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098334 | |||||||
chr5:133098350 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1929+1064C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098350 | |||||||
chr5:133098440 | T | G | 1 | a0001c0001t0001g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1930-1105T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098440 | |||||||
chr5:133098467 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1930-1078A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098467 | |||||||
chr5:133098470 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0334 |
2 | HG01255.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1930-1075C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098470 | |||||||
chr5:133098478 | AT | A | 147 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(144): Show |
150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1930-1053delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133098478 | ||||||
chr5:133098575 | G | A | 3 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 |
3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1930-970G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098575 | |||||||
chr5:133098634 | CTTTA | C | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-906_1930-903d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133098634 | ||||||
chr5:133098638 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1930-907A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098638 | |||||||
chr5:133098719 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(52): Show |
56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1930-826C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098719 | |||||||
chr5:133098769 | T | C | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1930-776T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098769 | |||||||
chr5:133098862 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0262 |
2 | NA18953.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1930-683G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098862 | |||||||
chr5:133098913 | C | G | 2 | a0001c0002t0018g0001 a0001c0002t0032g0029 |
3 | HG00323.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1930-632C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098913 | |||||||
chr5:133098916 | G | C | 14 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(11): Show |
14 | HG00438.hp1 NA18942.hp2 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.1930-629G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098916 | |||||||
chr5:133098957 | G | C | 70 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0012g0017 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1930-588G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098957 | |||||||
chr5:133099139 | AT | A | 6 | a0001c0001t0036g0015 a0001c0004t0011g0011 a0001c0004t0011g0013 others(3): Show |
6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930-398delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133099139 | ||||||
chr5:133099189 | G | A | 2 | a0001c0001t0008g0019 a0001c0001t0008g0020 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1930-356G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099189 | |||||||
chr5:133099190 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1930-355C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099190 | |||||||
chr5:133099195 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1930-350T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099195 | |||||||
chr5:133099270 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-275C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099270 | |||||||
chr5:133099314 | G | T | 1 | a0001c0001t0001g0333 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1930-231G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099314 | |||||||
chr5:133099411 | G | C | 20 | a0001c0001t0001g0085 a0001c0001t0001g0159 a0001c0001t0001g0160 others(17): Show |
20 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1930-134G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099411 | |||||||
chr5:133099417 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0300 a0001c0001t0001g0342 |
3 | HG00639.hp1 HG01069.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1930-128G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099417 | |||||||
chr5:133099454 | A | C | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0171 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-91A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099454 | |||||||
chr5:133099729 | T | A | 6 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0149 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2037+77T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133099729 | |||||||
chr5:133099796 | C | T | 62 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(59): Show |
64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.2037+144C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133099796 | |||||||
chr5:133099880 | C | T | 149 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(146): Show |
152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2037+228C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133099880 | |||||||
chr5:133100064 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2037+412T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100064 | |||||||
chr5:133100252 | CAG | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0184 |
3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2037+601_2037+602d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100252 | |||||||
chr5:133100261 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2037+609T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100261 | |||||||
chr5:133100482 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18953.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2037+830C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100482 | |||||||
chr5:133100527 | C | T | 63 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0002t0002g0002 others(60): Show |
65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.2037+875C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100527 | |||||||
chr5:133100636 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2037+984T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100636 | |||||||
chr5:133100645 | C | T | 1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2037+993C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100645 | |||||||
chr5:133100666 | T | C | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2037+1014T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100666 | |||||||
chr5:133100700 | C | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(150): Show |
156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.2037+1048C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100700 | |||||||
chr5:133100799 | T | G | 1 | a0001c0001t0001g0263 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2038-960T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100799 | |||||||
chr5:133101247 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2038-512C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133101247 | |||||||
chr5:133101560 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0142 a0001c0001t0001g0146 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038-199G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133101560 | |||||||
chr5:133101634 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2038-125A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133101634 | |||||||
chr5:133101718 | C | T | 1 | a0001c0002t0002g0071 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2038-41C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133101718 | |||||||
chr5:133101902 | C | T | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2157+24C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133101902 | |||||||
chr5:133101903 | T | A | 10 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
10 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2157+25T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133101903 | |||||||
chr5:133101904 | T | A | 10 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
10 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2157+26T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133101904 | |||||||
chr5:133101921 | C | CT | 17 | a0001c0001t0001g0141 a0001c0001t0001g0159 a0001c0001t0001g0164 others(14): Show |
17 | HG00280.hp1 HG01175.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2157+66dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | ||||||
chr5:133101921 | CT | C | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0148 others(25): Show |
28 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2157+66delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | ||||||
chr5:133101921 | CTT | C | 60 | a0001c0001t0001g0172 a0001c0001t0004g0076 a0001c0001t0005g0021 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2157+65_2157+66del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | ||||||
chr5:133101921 | CTTT | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(57): Show |
61 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.2157+64_2157+66del others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | ||||||
chr5:133101921 | CTTTTTTT others(5): Show |
C | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2157+55_2157+66del others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | ||||||
chr5:133101984 | T | C | 1 | a0001c0001t0012g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2157+106T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133101984 | |||||||
chr5:133102051 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2157+173C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102051 | |||||||
chr5:133102197 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2157+319C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102197 | |||||||
chr5:133102226 | C | T | 16 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2157+348C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102226 | |||||||
chr5:133102275 | G | C | 1 | a0001c0001t0008g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2157+397G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102275 | |||||||
chr5:133102343 | G | A | 57 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0190 others(54): Show |
57 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2157+465G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102343 | |||||||
chr5:133102372 | A | C | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2157+494A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102372 | |||||||
chr5:133102666 | C | T | 67 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(64): Show |
69 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.2157+788C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102666 | |||||||
chr5:133102689 | T | C | 1 | a0001c0001t0008g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2157+811T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102689 | |||||||
chr5:133102913 | C | CTTTTTTT others(1): Show |
60 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0351 others(57): Show |
61 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2158-942_2158-935d others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | ||||||
chr5:133102913 | C | CTTTTTTT others(2): Show |
17 | a0001c0001t0001g0085 a0001c0001t0001g0096 a0001c0001t0001g0130 others(14): Show |
17 | HG00639.hp2 HG01167.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2158-943_2158-935d others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | ||||||
chr5:133102913 | C | CTTTTTTT others(3): Show |
87 | a0001c0001t0001g0004 a0001c0001t0001g0086 a0001c0001t0001g0087 others(84): Show |
88 | HG00438.hp1 HG00558.hp1 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.2158-944_2158-935d others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | ||||||
chr5:133102913 | C | CTTTTTTT others(4): Show |
13 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG00609.hp2 HG01106.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2158-945_2158-935d others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | ||||||
chr5:133102913 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0082 a0001c0001t0022g0106 |
2 | HG03041.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2158-946_2158-935d others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | ||||||
chr5:133102913 | C | CTTTTTTT others(15): Show |
1 | a0007c0008t0029g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2158-935_2158-934i others(24): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | ||||||
chr5:133102993 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18974.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2158-872C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102993 | |||||||
chr5:133102996 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
6 | HG00099.hp2 HG00323.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.2158-869C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102996 | |||||||
chr5:133103008 | A | G | 6 | a0001c0001t0036g0015 a0001c0004t0011g0011 a0001c0004t0011g0013 others(3): Show |
6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2158-857A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103008 | |||||||
chr5:133103063 | T | C | 3 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 |
3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2158-802T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103063 | |||||||
chr5:133103070 | T | C | 7 | a0001c0001t0012g0017 a0001c0001t0036g0015 a0001c0004t0011g0011 others(4): Show |
7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2158-795T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103070 | |||||||
chr5:133103167 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2158-698C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103167 | |||||||
chr5:133103267 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(52): Show |
56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2158-598T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103267 | |||||||
chr5:133103278 | A | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(52): Show |
56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2158-587A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103278 | |||||||
chr5:133103318 | T | A | 74 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(71): Show |
76 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2158-547T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103318 | |||||||
chr5:133103318 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0016g0258 a0001c0001t0016g0259 |
3 | HG01123.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2158-547T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103318 | |||||||
chr5:133103336 | C | T | 67 | a0001c0001t0004g0076 a0001c0001t0005g0021 a0001c0001t0009g0350 others(64): Show |
69 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.2158-529C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103336 | |||||||
chr5:133103403 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2158-462C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103403 | |||||||
chr5:133103437 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2158-428C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103437 | |||||||
chr5:133103454 | C | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0219 a0001c0001t0001g0293 |
3 | NA18747.hp2 NA18970.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2158-411C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103454 | |||||||
chr5:133103470 | G | A | 1 | a0003c0005t0003g0166 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2158-395G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103470 | |||||||
chr5:133103682 | C | T | 1 | a0001c0002t0002g0038 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2158-183C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103682 | |||||||
chr5:133103810 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2158-55C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103810 | |||||||
chr5:133104046 | T | A | 4 | a0001c0001t0009g0350 a0001c0001t0009g0351 a0001c0001t0009g0352 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+20T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104046 | |||||||
chr5:133104063 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2319+37C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104063 | |||||||
chr5:133104115 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0337 |
2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2319+89A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104115 | |||||||
chr5:133104128 | C | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0082 others(52): Show |
56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2319+102C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104128 | |||||||
chr5:133104139 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2320-94A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104139 |