Links from Gene
Items: 1 to 20 of 1000
1.
rs1491564875 has merged into rs764981282 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 3:6715702
(GRCh38)
3:6757389
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
T=0.079/46
(NorthernSweden)
- HGVS:
NC_000003.12:g.6715702_6715706del, NC_000003.12:g.6715703_6715706del, NC_000003.12:g.6715704_6715706del, NC_000003.12:g.6715705_6715706del, NC_000003.12:g.6715706del, NC_000003.12:g.6715706dup, NC_000003.12:g.6715705_6715706dup, NC_000003.12:g.6715704_6715706dup, NC_000003.12:g.6715703_6715706dup, NC_000003.12:g.6715702_6715706dup, NC_000003.12:g.6715701_6715706dup, NC_000003.12:g.6715700_6715706dup, NC_000003.12:g.6715699_6715706dup, NC_000003.12:g.6715698_6715706dup, NC_000003.12:g.6715697_6715706dup, NC_000003.12:g.6715696_6715706dup, NC_000003.12:g.6715694_6715706dup, NC_000003.11:g.6757389_6757393del, NC_000003.11:g.6757390_6757393del, NC_000003.11:g.6757391_6757393del, NC_000003.11:g.6757392_6757393del, NC_000003.11:g.6757393del, NC_000003.11:g.6757393dup, NC_000003.11:g.6757392_6757393dup, NC_000003.11:g.6757391_6757393dup, NC_000003.11:g.6757390_6757393dup, NC_000003.11:g.6757389_6757393dup, NC_000003.11:g.6757388_6757393dup, NC_000003.11:g.6757387_6757393dup, NC_000003.11:g.6757386_6757393dup, NC_000003.11:g.6757385_6757393dup, NC_000003.11:g.6757384_6757393dup, NC_000003.11:g.6757383_6757393dup, NC_000003.11:g.6757381_6757393dup
2.
rs1491512664 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 3:6712642
(GRCh38)
3:6754329
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6712638:TATAT:TAT
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TAT=0./0
(
ALFA)
-=0.000008/2
(TOPMED)
-=0.000015/2
(GnomAD)
- HGVS:
3.
rs1491300566 has merged into rs143959345 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TCTCTCTCTCTCTCTC>-,TC,TCTC,TCTCTC,TCTCTCTC,TCTCTCTCTC,TCTCTCTCTCTC,TCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
[Show Flanks]
- Chromosome:
- 3:6714374
(GRCh38)
3:6756061
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000003.12:6714359:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TCTCTCTCTCTCTC=0./0
(
ALFA)
-=0.4784/2396
(1000Genomes)
- HGVS:
NC_000003.12:g.6714360TC[7], NC_000003.12:g.6714360TC[8], NC_000003.12:g.6714360TC[9], NC_000003.12:g.6714360TC[10], NC_000003.12:g.6714360TC[11], NC_000003.12:g.6714360TC[12], NC_000003.12:g.6714360TC[13], NC_000003.12:g.6714360TC[14], NC_000003.12:g.6714360TC[16], NC_000003.12:g.6714360TC[17], NC_000003.12:g.6714360TC[18], NC_000003.12:g.6714360TC[19], NC_000003.12:g.6714360TC[20], NC_000003.12:g.6714360TC[21], NC_000003.12:g.6714360TC[22], NC_000003.12:g.6714360TC[23], NC_000003.12:g.6714360TC[24], NC_000003.12:g.6714360TC[25], NC_000003.12:g.6714360TC[26], NC_000003.11:g.6756047TC[7], NC_000003.11:g.6756047TC[8], NC_000003.11:g.6756047TC[9], NC_000003.11:g.6756047TC[10], NC_000003.11:g.6756047TC[11], NC_000003.11:g.6756047TC[12], NC_000003.11:g.6756047TC[13], NC_000003.11:g.6756047TC[14], NC_000003.11:g.6756047TC[16], NC_000003.11:g.6756047TC[17], NC_000003.11:g.6756047TC[18], NC_000003.11:g.6756047TC[19], NC_000003.11:g.6756047TC[20], NC_000003.11:g.6756047TC[21], NC_000003.11:g.6756047TC[22], NC_000003.11:g.6756047TC[23], NC_000003.11:g.6756047TC[24], NC_000003.11:g.6756047TC[25], NC_000003.11:g.6756047TC[26]
4.
rs1491300445 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->ATTAATATATAATATATAATATGATTATA
[Show Flanks]
- Chromosome:
- 3:6712639
(GRCh38)
3:6754327
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6712639:ATATGATTATAATTAATATATAATATATAATATGATTATA:ATATGATTATAATTAATATATAATATATAATATGATTATAATTAATATATAATATATAATATGATTATA
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by cluster
- MAF:
ATATGATTATAATTAATATATAATATATA=0.000008/1
(GnomAD)
ATATGATTATAATTAATATATAATATATA=0.000177/3
(TOMMO)
- HGVS:
5.
rs1491281897 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TA>-
[Show Flanks]
- Chromosome:
- 3:6710166
(GRCh38)
3:6751853
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6710163:TATA:TA
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TATA=0./0
(
ALFA)
-=0.000007/1
(GnomAD)
-=0.001557/6
(ALSPAC)
-=0.001618/6
(TWINSUK)
- HGVS:
6.
rs1491205401 has merged into rs146390960 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AT>-,ATAT,ATATAT
[Show Flanks]
- Chromosome:
- 3:6710143
(GRCh38)
3:6751830
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6710134:ATATATATAT:ATATATAT,NC_000003.12:6710134:ATATATATAT:ATATATATATAT,NC_000003.12:6710134:ATATATATAT:ATATATATATATAT
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
ATATATATATATAT=0./0
(
ALFA)
-=0.05609/940
(TOMMO)
-=0.2524/1264
(1000Genomes)
-=0.30893/1384
(Estonian)
-=0.31363/313
(GoNL)
-=0.325/13
(GENOME_DK)
- HGVS:
8.
rs1491117569 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->GT
[Show Flanks]
- Chromosome:
- 3:6710135
(GRCh38)
3:6751823
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6710135:T:TGT
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
TGT=0.00008/1
(
ALFA)
TG=0.00001/1
(GnomAD)
- HGVS:
9.
rs1491022297 has merged into rs74750424 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 3:6709534
(GRCh38)
3:6751221
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:6709522:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTT=0./0
(
ALFA)
-=0.3794/1900
(1000Genomes)
- HGVS:
NC_000003.12:g.6709534_6709539del, NC_000003.12:g.6709535_6709539del, NC_000003.12:g.6709536_6709539del, NC_000003.12:g.6709537_6709539del, NC_000003.12:g.6709538_6709539del, NC_000003.12:g.6709539del, NC_000003.12:g.6709539dup, NC_000003.12:g.6709538_6709539dup, NC_000003.12:g.6709537_6709539dup, NC_000003.12:g.6709536_6709539dup, NC_000003.12:g.6709535_6709539dup, NC_000003.12:g.6709534_6709539dup, NC_000003.12:g.6709533_6709539dup, NC_000003.12:g.6709532_6709539dup, NC_000003.12:g.6709531_6709539dup, NC_000003.12:g.6709530_6709539dup, NC_000003.11:g.6751221_6751226del, NC_000003.11:g.6751222_6751226del, NC_000003.11:g.6751223_6751226del, NC_000003.11:g.6751224_6751226del, NC_000003.11:g.6751225_6751226del, NC_000003.11:g.6751226del, NC_000003.11:g.6751226dup, NC_000003.11:g.6751225_6751226dup, NC_000003.11:g.6751224_6751226dup, NC_000003.11:g.6751223_6751226dup, NC_000003.11:g.6751222_6751226dup, NC_000003.11:g.6751221_6751226dup, NC_000003.11:g.6751220_6751226dup, NC_000003.11:g.6751219_6751226dup, NC_000003.11:g.6751218_6751226dup, NC_000003.11:g.6751217_6751226dup
11.
rs1490848223 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 3:6707109
(GRCh38)
3:6748796
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6707108:C:T
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
12.
rs1490815599 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 3:6695075
(GRCh38)
3:6736762
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6695074:A:G
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,upstream_transcript_variant,genic_downstream_transcript_variant,genic_upstream_transcript_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.
rs1490768824 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 3:6706499
(GRCh38)
3:6748186
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6706498:A:G
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000014/2
(GnomAD)
- HGVS:
14.
rs1490713165 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A,T
[Show Flanks]
- Chromosome:
- 3:6725151
(GRCh38)
3:6766838
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6725150:C:A,NC_000003.12:6725150:C:T
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
A=0.000014/2
(GnomAD)
- HGVS:
15.
rs1490660784 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- T>-
[Show Flanks]
- Chromosome:
- 3:6706621
(GRCh38)
3:6748308
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6706620:TT:T
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
TT=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS:
16.
rs1490584324 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 3:6693352
(GRCh38)
3:6735039
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6693351:A:G
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,upstream_transcript_variant,genic_downstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000008/2
(TOPMED)
G=0.000014/2
(GnomAD)
- HGVS:
17.
rs1490474105 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->C
[Show Flanks]
- Chromosome:
- 3:6720971
(GRCh38)
3:6762659
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6720971::C
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000245/4
(
ALFA)
C=0.000071/1
(TOMMO)
C=0.00015/21
(GnomAD)
C=0.000312/2
(1000Genomes)
C=0.000446/2
(Estonian)
- HGVS:
18.
rs1490456264 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 3:6712532
(GRCh38)
3:6754219
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6712531:A:G
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000008/1
(GnomAD)
- HGVS:
19.
rs1490333037 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 3:6725050
(GRCh38)
3:6766737
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6725049:C:T
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000071/1
(
ALFA)
T=0.000008/2
(TOPMED)
T=0.000014/2
(GnomAD)
- HGVS:
20.
rs1490309319 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
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- Chromosome:
- 3:6713464
(GRCh38)
3:6755151
(GRCh37)
- Canonical SPDI:
- NC_000003.12:6713463:T:C
- Gene:
- GRM7-AS3 (Varview), LOC105376944 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000008/2
(TOPMED)
C=0.000495/8
(TOMMO)
C=0.000546/1
(Korea1K)
C=0.001027/3
(KOREAN)
- HGVS: