Links from Gene
Items: 1 to 20 of 29917
1.
rs1491554526 has merged into rs35233474 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTT>-,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 17:3369813
(GRCh38)
17:3273107
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3369805:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTT=0./0
(
ALFA)
-=0.4095/2051
(1000Genomes)
- HGVS:
NC_000017.11:g.3369813_3369821del, NC_000017.11:g.3369818_3369821del, NC_000017.11:g.3369819_3369821del, NC_000017.11:g.3369820_3369821del, NC_000017.11:g.3369821del, NC_000017.11:g.3369821dup, NC_000017.11:g.3369820_3369821dup, NC_000017.11:g.3369819_3369821dup, NC_000017.11:g.3369818_3369821dup, NC_000017.11:g.3369817_3369821dup, NC_000017.11:g.3369816_3369821dup, NC_000017.11:g.3369815_3369821dup, NC_000017.11:g.3369814_3369821dup, NC_000017.11:g.3369813_3369821dup, NC_000017.11:g.3369811_3369821dup, NC_000017.11:g.3369808_3369821dup, NC_000017.11:g.3369806_3369821T[31]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000017.11:g.3369821_3369822insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.3273107_3273115del, NC_000017.10:g.3273112_3273115del, NC_000017.10:g.3273113_3273115del, NC_000017.10:g.3273114_3273115del, NC_000017.10:g.3273115del, NC_000017.10:g.3273115dup, NC_000017.10:g.3273114_3273115dup, NC_000017.10:g.3273113_3273115dup, NC_000017.10:g.3273112_3273115dup, NC_000017.10:g.3273111_3273115dup, NC_000017.10:g.3273110_3273115dup, NC_000017.10:g.3273109_3273115dup, NC_000017.10:g.3273108_3273115dup, NC_000017.10:g.3273107_3273115dup, NC_000017.10:g.3273105_3273115dup, NC_000017.10:g.3273102_3273115dup, NC_000017.10:g.3273100_3273115T[31]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000017.10:g.3273115_3273116insTTTTTTTTTTTTTTTTTTTTTTTT
2.
rs1491539867 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CA>-
[Show Flanks]
- Chromosome:
- 17:3306679
(GRCh38)
17:3209973
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3306678:CA:
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0.00067/8
(
ALFA)
-=0.00027/14
(GnomAD)
-=0.08198/304
(TWINSUK)
-=0.08744/337
(ALSPAC)
- HGVS:
3.
rs1491538736 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->C
[Show Flanks]
- Chromosome:
- 17:3375140
(GRCh38)
17:3278435
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3375140::C
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.00152/71
(GnomAD)
- HGVS:
5.
rs1491502799 has merged into rs552615698 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 17:3375150
(GRCh38)
17:3278444
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:3375139:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000017.11:g.3375150_3375169del, NC_000017.11:g.3375151_3375169del, NC_000017.11:g.3375152_3375169del, NC_000017.11:g.3375153_3375169del, NC_000017.11:g.3375154_3375169del, NC_000017.11:g.3375155_3375169del, NC_000017.11:g.3375156_3375169del, NC_000017.11:g.3375157_3375169del, NC_000017.11:g.3375158_3375169del, NC_000017.11:g.3375159_3375169del, NC_000017.11:g.3375160_3375169del, NC_000017.11:g.3375161_3375169del, NC_000017.11:g.3375162_3375169del, NC_000017.11:g.3375163_3375169del, NC_000017.11:g.3375164_3375169del, NC_000017.11:g.3375165_3375169del, NC_000017.11:g.3375166_3375169del, NC_000017.11:g.3375167_3375169del, NC_000017.11:g.3375168_3375169del, NC_000017.11:g.3375169del, NC_000017.11:g.3375169dup, NC_000017.11:g.3375168_3375169dup, NC_000017.11:g.3375167_3375169dup, NC_000017.11:g.3375166_3375169dup, NC_000017.11:g.3375165_3375169dup, NC_000017.11:g.3375164_3375169dup, NC_000017.11:g.3375163_3375169dup, NC_000017.11:g.3375162_3375169dup, NC_000017.11:g.3375160_3375169dup, NC_000017.11:g.3375159_3375169dup, NC_000017.11:g.3375155_3375169dup, NC_000017.11:g.3375154_3375169dup, NC_000017.11:g.3375153_3375169dup, NC_000017.11:g.3375152_3375169dup, NC_000017.11:g.3375151_3375169dup, NC_000017.11:g.3375150_3375169dup, NC_000017.11:g.3375149_3375169dup, NC_000017.11:g.3375147_3375169dup, NC_000017.11:g.3375146_3375169dup, NC_000017.11:g.3375145_3375169dup, NC_000017.11:g.3375143_3375169dup, NC_000017.11:g.3375141_3375169dup, NC_000017.11:g.3375140_3375169dup, NC_000017.11:g.3375169_3375170insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.11:g.3375169_3375170insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.11:g.3375169_3375170insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.11:g.3375169_3375170insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.11:g.3375169_3375170insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.11:g.3375169_3375170insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.11:g.3375169_3375170insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.3278444_3278463del, NC_000017.10:g.3278445_3278463del, NC_000017.10:g.3278446_3278463del, NC_000017.10:g.3278447_3278463del, NC_000017.10:g.3278448_3278463del, NC_000017.10:g.3278449_3278463del, NC_000017.10:g.3278450_3278463del, NC_000017.10:g.3278451_3278463del, NC_000017.10:g.3278452_3278463del, NC_000017.10:g.3278453_3278463del, NC_000017.10:g.3278454_3278463del, NC_000017.10:g.3278455_3278463del, NC_000017.10:g.3278456_3278463del, NC_000017.10:g.3278457_3278463del, NC_000017.10:g.3278458_3278463del, NC_000017.10:g.3278459_3278463del, NC_000017.10:g.3278460_3278463del, NC_000017.10:g.3278461_3278463del, NC_000017.10:g.3278462_3278463del, NC_000017.10:g.3278463del, NC_000017.10:g.3278463dup, NC_000017.10:g.3278462_3278463dup, NC_000017.10:g.3278461_3278463dup, NC_000017.10:g.3278460_3278463dup, NC_000017.10:g.3278459_3278463dup, NC_000017.10:g.3278458_3278463dup, NC_000017.10:g.3278457_3278463dup, NC_000017.10:g.3278456_3278463dup, NC_000017.10:g.3278454_3278463dup, NC_000017.10:g.3278453_3278463dup, NC_000017.10:g.3278449_3278463dup, NC_000017.10:g.3278448_3278463dup, NC_000017.10:g.3278447_3278463dup, NC_000017.10:g.3278446_3278463dup, NC_000017.10:g.3278445_3278463dup, NC_000017.10:g.3278444_3278463dup, NC_000017.10:g.3278443_3278463dup, NC_000017.10:g.3278441_3278463dup, NC_000017.10:g.3278440_3278463dup, NC_000017.10:g.3278439_3278463dup, NC_000017.10:g.3278437_3278463dup, NC_000017.10:g.3278435_3278463dup, NC_000017.10:g.3278434_3278463dup, NC_000017.10:g.3278463_3278464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.3278463_3278464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.3278463_3278464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.3278463_3278464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.3278463_3278464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.3278463_3278464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.3278463_3278464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
6.
rs1491452518 has merged into rs61331985 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ATATAT>-,AT,ATAT,ATATATAT,ATATATATAT
[Show Flanks]
- Chromosome:
- 17:3304008
(GRCh38)
17:3207302
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3303995:ATATATATATATATATAT:ATATATATATAT,NC_000017.11:3303995:ATATATATATATATATAT:ATATATATATATAT,NC_000017.11:3303995:ATATATATATATATATAT:ATATATATATATATAT,NC_000017.11:3303995:ATATATATATATATATAT:ATATATATATATATATATAT,NC_000017.11:3303995:ATATATATATATATATAT:ATATATATATATATATATATAT
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
ATATATATATATATATATAT=0./0
(
ALFA)
AT=0.0455/228
(1000Genomes)
-=0.0944/364
(ALSPAC)
- HGVS:
7.
rs1491441030 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 17:3369805
(GRCh38)
17:3273099
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3369804:CT:
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0.00008/1
(
ALFA)
-=0.00007/5
(GnomAD)
- HGVS:
8.
rs1491431268 has merged into rs1359379744 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AG>-,AGAG
[Show Flanks]
- Chromosome:
- 17:3372906
(GRCh38)
17:3276200
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3372902:GAGAG:GAG,NC_000017.11:3372902:GAGAG:GAGAGAG
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
GAGAGAG=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
GA=0.000037/5
(GnomAD)
- HGVS:
9.
rs1491395746 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 17:3288545
(GRCh38)
17:3191839
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3288544:AT:
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0./0
(
ALFA)
-=0.000008/2
(TOPMED)
- HGVS:
10.
rs1491373841 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 17:3295023
(GRCh38)
17:3198317
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3295020:CTCT:CT
- Gene:
- OR3A1 (Varview), OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CTCT=0./0
(
ALFA)
-=0.000029/4
(GnomAD)
-=0.00003/8
(TOPMED)
- HGVS:
11.
rs1491299191 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->ACTG
[Show Flanks]
- Chromosome:
- 17:3288545
(GRCh38)
17:3191840
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3288545:TGACTG:TGACTGACTG
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TGACTGACTG=0./0
(
ALFA)
TGAC=0.000057/8
(GnomAD)
TGAC=0.000091/24
(TOPMED)
TGAC=0.000156/1
(1000Genomes)
- HGVS:
12.
rs1491267870 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GT>-
[Show Flanks]
- Chromosome:
- 17:3283022
(GRCh38)
17:3186316
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3283020:TGT:T
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
-=0.00003/4
(GnomAD)
- HGVS:
13.
rs1491244680 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->CT
[Show Flanks]
- Chromosome:
- 17:3375138
(GRCh38)
17:3278433
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3375138:CT:CTCT
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CTCT=0.00069/3
(
ALFA)
CT=0.0005/17
(GnomAD)
- HGVS:
14.
rs1491214194 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 17:3375300
(GRCh38)
17:3278594
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3375299:CT:
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0./0
(
ALFA)
-=0.00001/1
(GnomAD)
- HGVS:
16.
rs1491162600 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->AAGAGG
[Show Flanks]
- Chromosome:
- 17:3372903
(GRCh38)
17:3276198
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3372903:AGAGG:AGAGGAAGAGG
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency
- MAF:
AGAGGA=0.000008/1
(GnomAD)
- HGVS:
17.
rs1491152663 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->T
[Show Flanks]
- Chromosome:
- 17:3295021
(GRCh38)
17:3198316
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3295021:T:TT
- Gene:
- OR3A1 (Varview), OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TT=0.000285/4
(
ALFA)
T=0.000076/20
(TOPMED)
T=0.0001/14
(GnomAD)
T=0.000156/1
(1000Genomes)
- HGVS:
18.
rs1491120536 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->A
[Show Flanks]
- Chromosome:
- 17:3369806
(GRCh38)
17:3273101
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3369806::A
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000195/3
(GnomAD)
- HGVS:
19.
rs1491072489 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->CAAAAAAAA
[Show Flanks]
- Chromosome:
- 17:3306681
(GRCh38)
17:3209976
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3306681:AAAAAAAA:AAAAAAAACAAAAAAAA
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
AAAAAAAACAAAAAAAA=0./0
(
ALFA)
- HGVS:
20.
rs1491060098 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TA>-
[Show Flanks]
- Chromosome:
- 17:3345440
(GRCh38)
17:3248734
(GRCh37)
- Canonical SPDI:
- NC_000017.11:3345438:ATA:A
- Gene:
- OR3A2 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0.000169/2
(
ALFA)
-=0.000049/6
(GnomAD)
- HGVS: