regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | 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 | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
STON2_chr14_81255652_81405324 | 81320429 | G | GACCATTT others(2698): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0034 | 1 | 264 | 0.0038 | 2705 | c.742 others(2722): Show |
STON2 | ENSG00000140022.14 | transcript | ENST00000614646.5 | protein_coding | 5/7 | chr14 | TogoVar | ||||||
TAF11L10_chr5_17592232_17602828 | 17598414 | T | TCTCCCAC others(2698): Show |
upstream_gene_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0000 | a0001c0001t0000g0000 | 1 | 352 | 0.0028 | 2705 | c.-58 others(2714): Show |
TAF11L10 | ENSG00000284356.1 | transcript | ENST00000638842.1 | protein_coding | 587 | chr5 | TogoVar | ||||||
TAF11L9_chr5_17588798_17599394 | 17598414 | T | TCTCCCAC others(2698): Show |
upstream_gene_variant | MODIFIER | NA19065.hp1 | a0001 | a0001c0001 | a0001c0001t0000 | a0001c0001t0000g0000 | 1 | 112 | 0.0089 | 2705 | c.-40 others(2716): Show |
TAF11L9 | ENSG00000283988.1 | transcript | ENST00000639969.1 | protein_coding | 4021 | chr5 | TogoVar | ||||||
TAF11L9_chr5_17588798_17599394 | 17598414 | T | TCTCCCAC others(2698): Show |
upstream_gene_variant | MODIFIER | NA19009.hp2 | a0001 | a0001c0001 | a0001c0001t0000 | a0001c0001t0000g0000 | 1 | 112 | 0.0089 | 2705 | c.-40 others(2716): Show |
TAF11L9 | ENSG00000283988.1 | transcript | ENST00000639969.1 | protein_coding | 4021 | chr5 | TogoVar | ||||||
TAF11L9_chr5_17588798_17599394 | 17598414 | T | TCTCCCAC others(2698): Show |
upstream_gene_variant | MODIFIER | NA18978.hp1 | a0001 | a0001c0001 | a0001c0001t0000 | a0001c0001t0000g0000 | 1 | 112 | 0.0089 | 2705 | c.-40 others(2716): Show |
TAF11L9 | ENSG00000283988.1 | transcript | ENST00000639969.1 | protein_coding | 4021 | chr5 | TogoVar | ||||||
TAF11L9_chr5_17588798_17599394 | 17598414 | T | TCTCCCAC others(2698): Show |
upstream_gene_variant | MODIFIER | NA18981.hp1 | a0001 | a0001c0001 | a0001c0001t0000 | a0001c0001t0000g0000 | 1 | 112 | 0.0089 | 2705 | c.-40 others(2716): Show |
TAF11L9 | ENSG00000283988.1 | transcript | ENST00000639969.1 | protein_coding | 4021 | chr5 | TogoVar | ||||||
CRIP2_chr14_105469821_105485162 | 105477719 | G | GGGGAAGC others(2699): Show |
intron_variant | MODIFIER | HG02145.hp1 HG03710.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0249 | 2 | 316 | 0.0063 | 2706 | c.44- others(2719): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
CRIP2_chr14_105469821_105485162 | 105477719 | G | GGGGAAGC others(2699): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0242 | 1 | 316 | 0.0032 | 2706 | c.44- others(2719): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
FAM118A_chr22_45304934_45346955 | 45328345 | G | GGCAGAAC others(2699): Show |
intron_variant | MODIFIER | HG01952.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0150 | 1 | 416 | 0.0024 | 2706 | c.522 others(2721): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
HPCAL1_chr2_10297904_10432604 | 10399271 | C | CCACCACC others(2699): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0284 | 1 | 314 | 0.0032 | 2706 | c.-25 others(2723): Show |
HPCAL1 | ENSG00000115756.13 | transcript | ENST00000307845.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
LMF1_chr16_848634_975984 | 859712 | C | CGGGTGTG others(2699): Show |
intron_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228 | 1 | 294 | 0.0034 | 2706 | c.153 others(2725): Show |
LMF1 | ENSG00000103227.19 | transcript | ENST00000262301.16 | protein_coding | 10/10 | chr16 | TogoVar | ||||||
LMF1_chr16_848634_975984 | 859736 | C | CGGGTGTG others(2699): Show |
intron_variant | MODIFIER | HG02165.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0173 | 1 | 294 | 0.0034 | 2706 | c.153 others(2725): Show |
LMF1 | ENSG00000103227.19 | transcript | ENST00000262301.16 | protein_coding | 10/10 | chr16 | TogoVar | ||||||
LMF1_chr16_848634_975984 | 859759 | A | ATGGGTGT others(2699): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0261 | 1 | 294 | 0.0034 | 2706 | c.153 others(2725): Show |
LMF1 | ENSG00000103227.19 | transcript | ENST00000262301.16 | protein_coding | 10/10 | chr16 | TogoVar | ||||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | NA18994.hp2 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0276 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | NA19087.hp1 | a0001 | a0001c0004 | a0001c0004t0008 | a0001c0004t0008g0172 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0151 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG01255.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0220 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00597.hp2 NA18939.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(1): Show | 4 | 295 | 0.0136 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0224 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG02165.hp2 NA18957.hp2 NA18964.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0050 | a0001c0001t0001g0159a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | 295 | 0.0170 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | NA18979.hp2 | a0001 | a0001c0004 | a0001c0004t0011 | a0001c0004t0011g0062 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | NA18954.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0144 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0236 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG02027.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0238 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(48): Show |
a0001a0007a0009 | a0001c0001a0001c0004a0007c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0001g0161others(48): Show | 51 | 295 | 0.1729 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0001 | a0001c0001t0061 | a0001c0001t0061g0241 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | NA20805.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0206 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0222 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | NA18970.hp1 NA18982.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0115a0001c0001t0001g0165 | 2 | 295 | 0.0068 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | NA18973.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RAB11FIP3_chr16_420649_528011 | 494827 | T | TGGGAGGT others(2699): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072 | 1 | 295 | 0.0034 | 2706 | c.126 others(2725): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SLC25A18_chr22_17558498_17595995 | 17577684 | C | CATTCTCC others(2699): Show |
intron_variant | MODIFIER | HG02300.hp1 NA19083.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0281a0001c0001t0002g0096 | 2 | 410 | 0.0049 | 2706 | c.-20 others(2725): Show |
SLC25A18 | ENSG00000182902.14 | transcript | ENST00000327451.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
SLC25A18_chr22_17558498_17595995 | 17577684 | C | CATTCTCC others(2699): Show |
intron_variant | MODIFIER | NA18942.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0099 | 1 | 410 | 0.0024 | 2706 | c.-20 others(2725): Show |
SLC25A18 | ENSG00000182902.14 | transcript | ENST00000327451.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
SLC25A18_chr22_17558498_17595995 | 17577684 | C | CATTCTCC others(2699): Show |
intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0161 | 1 | 410 | 0.0024 | 2706 | c.-20 others(2725): Show |
SLC25A18 | ENSG00000182902.14 | transcript | ENST00000327451.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
SLC25A18_chr22_17558498_17595995 | 17577684 | C | CATTCTCC others(2699): Show |
intron_variant | MODIFIER | HG01167.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0272 | 1 | 410 | 0.0024 | 2706 | c.-20 others(2725): Show |
SLC25A18 | ENSG00000182902.14 | transcript | ENST00000327451.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
SLC25A18_chr22_17558498_17595995 | 17577684 | C | CATTCTCC others(2699): Show |
intron_variant | MODIFIER | HG00639.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0178 | 1 | 410 | 0.0024 | 2706 | c.-20 others(2725): Show |
SLC25A18 | ENSG00000182902.14 | transcript | ENST00000327451.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
SLC25A18_chr22_17558498_17595995 | 17577684 | C | CATTCTCC others(2699): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0203 | 1 | 410 | 0.0024 | 2706 | c.-20 others(2725): Show |
SLC25A18 | ENSG00000182902.14 | transcript | ENST00000327451.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
SLC25A18_chr22_17558498_17595995 | 17577684 | C | CATTCTCC others(2699): Show |
intron_variant | MODIFIER | NA18981.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0142 | 1 | 410 | 0.0024 | 2706 | c.-20 others(2725): Show |
SLC25A18 | ENSG00000182902.14 | transcript | ENST00000327451.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
SLC25A18_chr22_17558498_17595995 | 17577684 | C | CATTCTCC others(2699): Show |
intron_variant | MODIFIER | NA18951.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0256 | 1 | 410 | 0.0024 | 2706 | c.-20 others(2725): Show |
SLC25A18 | ENSG00000182902.14 | transcript | ENST00000327451.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
SPAAR_chr9_35904490_35916686 | 35913964 | T | TAGTGTGT others(2699): Show |
downstream_gene_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0003 | 1 | 420 | 0.0024 | 2706 | c.*32 others(2717): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2279 | chr9 | TogoVar | ||||||
SPAAR_chr9_35904490_35916686 | 35913964 | T | TAGTGTGT others(2699): Show |
downstream_gene_variant | MODIFIER | NA18944.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0012 | 1 | 420 | 0.0024 | 2706 | c.*32 others(2717): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2279 | chr9 | TogoVar | ||||||
SPAAR_chr9_35904490_35916686 | 35913964 | T | TAGTGTGT others(2699): Show |
downstream_gene_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0001 | 1 | 420 | 0.0024 | 2706 | c.*32 others(2717): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2279 | chr9 | TogoVar | ||||||
STON2_chr14_81255652_81405324 | 81320429 | G | GACCATTT others(2699): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0005 | a0005c0005 | a0005c0005t0004 | a0005c0005t0004g0090 | 1 | 264 | 0.0038 | 2706 | c.742 others(2723): Show |
STON2 | ENSG00000140022.14 | transcript | ENST00000614646.5 | protein_coding | 5/7 | chr14 | TogoVar | ||||||
STON2_chr14_81255652_81405324 | 81320429 | G | GACCATTT others(2699): Show |
intron_variant | MODIFIER | HG01257.hp1 HG02895.hp2 NA18957.hp2 others(1): Show |
a0004 | a0004c0004 | a0004c0004t0006a0004c0004t0017a0004c0004t0047 | a0004c0004t0006g0003a0004c0004t0006g0069a0004c0004t0017g0052others(1): Show | 4 | 264 | 0.0152 | 2706 | c.742 others(2723): Show |
STON2 | ENSG00000140022.14 | transcript | ENST00000614646.5 | protein_coding | 5/7 | chr14 | TogoVar | ||||||
STON2_chr14_81255652_81405324 | 81320429 | G | GACCATTT others(2699): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0058 | 1 | 264 | 0.0038 | 2706 | c.742 others(2723): Show |
STON2 | ENSG00000140022.14 | transcript | ENST00000614646.5 | protein_coding | 5/7 | chr14 | TogoVar | ||||||
STON2_chr14_81255652_81405324 | 81320429 | G | GACCATTT others(2699): Show |
intron_variant | MODIFIER | HG02970.hp1 NA19240.hp2 |
a0005a0006 | a0005c0005a0006c0011 | a0005c0005t0004a0006c0011t0015 | a0005c0005t0004g0002a0006c0011t0015g0208 | 2 | 264 | 0.0076 | 2706 | c.742 others(2723): Show |
STON2 | ENSG00000140022.14 | transcript | ENST00000614646.5 | protein_coding | 5/7 | chr14 | TogoVar | ||||||
ABCC2_chr10_99777640_99857594 | 99838928 | T | TCCCGGAC others(2700): Show |
intron_variant | MODIFIER | HG02071.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0214 | 1 | 336 | 0.0030 | 2707 | c.361 others(2726): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
AHRR_chr5_316714_443285 | 344505 | T | TGTGTGTG others(2700): Show |
intron_variant | MODIFIER | HG03491.hp1 HG03492.hp1 |
a0003 | a0003c0004 | a0003c0004t0004 | a0003c0004t0004g0164a0003c0004t0004g0169 | 2 | 268 | 0.0075 | 2707 | c.62+ others(2720): Show |
AHRR | ENSG00000063438.20 | transcript | ENST00000684583.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FOXK2_chr17_82514732_82609602 | 82586451 | G | GGGGGGGA others(2700): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0010 | 1 | 308 | 0.0033 | 2707 | c.157 others(2724): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
GALNT9_chr12_132191372_132334589 | 132243320 | A | AACACACC others(2700): Show |
intron_variant | MODIFIER | NA19002.hp2 | a0003 | a0003c0033 | a0003c0033t0001 | a0003c0033t0001g0114 | 1 | 183 | 0.0055 | 2707 | c.107 others(2726): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar |