Links from Gene
Items: 1 to 20 of 1000
3.
rs1491467797 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 8:11343878
(GRCh38)
8:11201387
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11343877:CT:
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000008/2
(TOPMED)
-=0.000014/2
(GnomAD)
- HGVS:
5.
rs1491249676 has merged into rs1158772046 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TATATATATATATATATATATATATATATATATATATATATATA>-,TA,TATA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
[Show Flanks]
- Chromosome:
- 8:11345871
(GRCh38)
8:11203380
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:11345858:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
- Gene:
- TDH (Varview), TDH-AS1 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000008.11:g.11345859TA[6], NC_000008.11:g.11345859TA[7], NC_000008.11:g.11345859TA[8], NC_000008.11:g.11345859TA[9], NC_000008.11:g.11345859TA[10], NC_000008.11:g.11345859TA[11], NC_000008.11:g.11345859TA[12], NC_000008.11:g.11345859TA[13], NC_000008.11:g.11345859TA[14], NC_000008.11:g.11345859TA[15], NC_000008.11:g.11345859TA[16], NC_000008.11:g.11345859TA[17], NC_000008.11:g.11345859TA[18], NC_000008.11:g.11345859TA[19], NC_000008.11:g.11345859TA[20], NC_000008.11:g.11345859TA[21], NC_000008.11:g.11345859TA[22], NC_000008.11:g.11345859TA[23], NC_000008.11:g.11345859TA[24], NC_000008.11:g.11345859TA[25], NC_000008.11:g.11345859TA[26], NC_000008.11:g.11345859TA[27], NC_000008.11:g.11345859TA[29], NC_000008.11:g.11345859TA[30], NC_000008.11:g.11345859TA[31], NC_000008.11:g.11345859TA[32], NC_000008.11:g.11345859TA[33], NC_000008.11:g.11345859TA[36], NC_000008.10:g.11203368TA[6], NC_000008.10:g.11203368TA[7], NC_000008.10:g.11203368TA[8], NC_000008.10:g.11203368TA[9], NC_000008.10:g.11203368TA[10], NC_000008.10:g.11203368TA[11], NC_000008.10:g.11203368TA[12], NC_000008.10:g.11203368TA[13], NC_000008.10:g.11203368TA[14], NC_000008.10:g.11203368TA[15], NC_000008.10:g.11203368TA[16], NC_000008.10:g.11203368TA[17], NC_000008.10:g.11203368TA[18], NC_000008.10:g.11203368TA[19], NC_000008.10:g.11203368TA[20], NC_000008.10:g.11203368TA[21], NC_000008.10:g.11203368TA[22], NC_000008.10:g.11203368TA[23], NC_000008.10:g.11203368TA[24], NC_000008.10:g.11203368TA[25], NC_000008.10:g.11203368TA[26], NC_000008.10:g.11203368TA[27], NC_000008.10:g.11203368TA[29], NC_000008.10:g.11203368TA[30], NC_000008.10:g.11203368TA[31], NC_000008.10:g.11203368TA[32], NC_000008.10:g.11203368TA[33], NC_000008.10:g.11203368TA[36], NW_018654717.1:g.2000934_2000935insTATAT, NW_018654717.1:g.2000935_2000973del, NW_018654717.1:g.2000935_2000971del, NW_018654717.1:g.2000935_2000969del, NW_018654717.1:g.2000935_2000967del, NW_018654717.1:g.2000935_2000965del, NW_018654717.1:g.2000935_2000963del, NW_018654717.1:g.2000935_2000961del, NW_018654717.1:g.2000935_2000959del, NW_018654717.1:g.2000935_2000957del, NW_018654717.1:g.2000935_2000955del, NW_018654717.1:g.2000935_2000953del, NW_018654717.1:g.2000935_2000951del, NW_018654717.1:g.2000935_2000949del, NW_018654717.1:g.2000935_2000947del, NW_018654717.1:g.2000935_2000945del, NW_018654717.1:g.2000935_2000943del, NW_018654717.1:g.2000935_2000941del, NW_018654717.1:g.2000935_2000939del, NW_018654717.1:g.2000935_2000937del, NW_018654717.1:g.2000935del, NW_018654717.1:g.2000934dup, NW_018654717.1:g.2000934_2000935insTAT, NW_018654717.1:g.2000934_2000935insTATATAT, NW_018654717.1:g.2000934_2000935insTATATATAT, NW_018654717.1:g.2000934_2000935insTATATATATAT, NW_018654717.1:g.2000934_2000935insTATATATATATAT, NW_018654717.1:g.2000934_2000935insTATATATATATATAT, NW_018654717.1:g.2000934_2000935insTATATATATATATATATATAT, NR_147705.1:n.947TA[6], NR_147705.1:n.947TA[7], NR_147705.1:n.947TA[8], NR_147705.1:n.947TA[9], NR_147705.1:n.947TA[10], NR_147705.1:n.947TA[11], NR_147705.1:n.947TA[12], NR_147705.1:n.947TA[13], NR_147705.1:n.947TA[14], NR_147705.1:n.947TA[15], NR_147705.1:n.947TA[16], NR_147705.1:n.947TA[17], NR_147705.1:n.947TA[18], NR_147705.1:n.947TA[19], NR_147705.1:n.947TA[20], NR_147705.1:n.947TA[21], NR_147705.1:n.947TA[22], NR_147705.1:n.947TA[23], NR_147705.1:n.947TA[24], NR_147705.1:n.947TA[25], NR_147705.1:n.947TA[26], NR_147705.1:n.947TA[27], NR_147705.1:n.947TA[29], NR_147705.1:n.947TA[30], NR_147705.1:n.947TA[31], NR_147705.1:n.947TA[32], NR_147705.1:n.947TA[33], NR_147705.1:n.947TA[36]
6.
rs1491245635 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->TGCACACA
[Show Flanks]
- Chromosome:
- 8:11360285
(GRCh38)
8:11217795
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11360285:CACACA:CACACATGCACACA
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
CACACATGCACACA=0.000084/1
(
ALFA)
CACACATG=0.000047/5
(GnomAD)
- HGVS:
7.
rs1491231683 has merged into rs35750076 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 8:11344111
(GRCh38)
8:11201620
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTTTT=0./0
(
ALFA)
TT=0.4681/2344
(1000Genomes)
- HGVS:
NC_000008.11:g.11344111_11344116del, NC_000008.11:g.11344113_11344116del, NC_000008.11:g.11344114_11344116del, NC_000008.11:g.11344115_11344116del, NC_000008.11:g.11344116del, NC_000008.11:g.11344116dup, NC_000008.11:g.11344115_11344116dup, NC_000008.11:g.11344114_11344116dup, NC_000008.11:g.11344107_11344116dup, NC_000008.10:g.11201620_11201625del, NC_000008.10:g.11201622_11201625del, NC_000008.10:g.11201623_11201625del, NC_000008.10:g.11201624_11201625del, NC_000008.10:g.11201625del, NC_000008.10:g.11201625dup, NC_000008.10:g.11201624_11201625dup, NC_000008.10:g.11201623_11201625dup, NC_000008.10:g.11201616_11201625dup, NW_018654717.1:g.2002742_2002747del, NW_018654717.1:g.2002744_2002747del, NW_018654717.1:g.2002745_2002747del, NW_018654717.1:g.2002746_2002747del, NW_018654717.1:g.2002747del, NW_018654717.1:g.2002747dup, NW_018654717.1:g.2002746_2002747dup, NW_018654717.1:g.2002745_2002747dup, NW_018654717.1:g.2002738_2002747dup
8.
rs1490999147 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- 8:11365756
(GRCh38)
8:11223265
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11365755:C:G
- Gene:
- TDH (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000007/1
(GnomAD)
G=0.000015/4
(TOPMED)
- HGVS:
9.
rs1490906575 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 8:11363172
(GRCh38)
8:11220681
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11363171:C:T
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
T=0.000156/1
(1000Genomes)
- HGVS:
10.
rs1490863267 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 8:11353192
(GRCh38)
8:11210701
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11353191:G:C
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000007/1
(GnomAD)
- HGVS:
11.
rs1490850060 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 8:11362436
(GRCh38)
8:11219945
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11362435:G:T
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000071/1
(
ALFA)
T=0.000007/1
(GnomAD)
T=0.000019/5
(TOPMED)
- HGVS:
12.
rs1490817164 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G,T
[Show Flanks]
- Chromosome:
- 8:11352274
(GRCh38)
8:11209783
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11352273:C:G,NC_000008.11:11352273:C:T
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000007/1
(GnomAD)
- HGVS:
13.
rs1490755944 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 8:11341140
(GRCh38)
8:11198649
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11341139:A:G
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.00004/1
(TOMMO)
- HGVS:
14.
rs1490730350 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 8:11339882
(GRCh38)
8:11197391
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11339881:G:A
- Gene:
- MTMR9 (Varview), TDH (Varview)
- Functional Consequence:
- 500B_downstream_variant,downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000029/4
(GnomAD)
A=0.000034/9
(TOPMED)
A=0.000035/1
(TOMMO)
A=0.000468/3
(1000Genomes)
A=0.000546/1
(Korea1K)
A=0.000684/2
(KOREAN)
- HGVS:
15.
rs1490665929 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 8:11343392
(GRCh38)
8:11200901
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11343391:C:T
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
16.
rs1490649783 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 8:11352680
(GRCh38)
8:11210189
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11352679:T:C
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
17.
rs1490570914 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A
[Show Flanks]
- Chromosome:
- 8:11342524
(GRCh38)
8:11200033
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11342523:C:A
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
A=0.000019/5
(TOPMED)
- HGVS:
18.
rs1490545948 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 8:11353690
(GRCh38)
8:11211199
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11353689:A:G
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0.000071/1
(
ALFA)
G=0.000007/1
(GnomAD)
- HGVS:
19.
rs1490509692 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 8:11365007
(GRCh38)
8:11222516
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11365006:A:T
- Gene:
- TDH (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000264/4
(
ALFA)
T=0.000029/4
(GnomAD)
T=0.000893/4
(Estonian)
- HGVS:
20.
rs1490485086 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- 8:11368348
(GRCh38)
8:11225857
(GRCh37)
- Canonical SPDI:
- NC_000008.11:11368347:C:G
- Gene:
- FAM167A-AS1 (Varview), TDH (Varview)
- Functional Consequence:
- 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000007/1
(GnomAD)
G=0.000011/3
(TOPMED)
- HGVS: