Links from Gene
Items: 1 to 20 of 20228
2.
rs1491571225 has merged into rs34095541 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTT>-,T,TT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTGTTTGGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:10914749
(GRCh38)
6:10914982
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTGGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
T=0.1957/980
(1000Genomes)
- HGVS:
NC_000006.12:g.10914749_10914759del, NC_000006.12:g.10914750_10914759del, NC_000006.12:g.10914751_10914759del, NC_000006.12:g.10914755_10914759del, NC_000006.12:g.10914756_10914759del, NC_000006.12:g.10914757_10914759del, NC_000006.12:g.10914758_10914759del, NC_000006.12:g.10914759del, NC_000006.12:g.10914759dup, NC_000006.12:g.10914758_10914759dup, NC_000006.12:g.10914757_10914759dup, NC_000006.12:g.10914756_10914759dup, NC_000006.12:g.10914755_10914759dup, NC_000006.12:g.10914754_10914759dup, NC_000006.12:g.10914752_10914759dup, NC_000006.12:g.10914739_10914759T[29]GTTTGGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.10914759_10914760insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10914982_10914992del, NC_000006.11:g.10914983_10914992del, NC_000006.11:g.10914984_10914992del, NC_000006.11:g.10914988_10914992del, NC_000006.11:g.10914989_10914992del, NC_000006.11:g.10914990_10914992del, NC_000006.11:g.10914991_10914992del, NC_000006.11:g.10914992del, NC_000006.11:g.10914992dup, NC_000006.11:g.10914991_10914992dup, NC_000006.11:g.10914990_10914992dup, NC_000006.11:g.10914989_10914992dup, NC_000006.11:g.10914988_10914992dup, NC_000006.11:g.10914987_10914992dup, NC_000006.11:g.10914985_10914992dup, NC_000006.11:g.10914972_10914992T[29]GTTTGGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.10914992_10914993insTTTTTTTTTTTTTTTTTTTTTTTTTT
3.
rs1491567450 has merged into rs58800098 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:10911904
(GRCh38)
6:10912137
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10911894:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTT=0./0
(
ALFA)
-=0.18963/4740
(TOMMO)
- HGVS:
NC_000006.12:g.10911904_10911919del, NC_000006.12:g.10911906_10911919del, NC_000006.12:g.10911907_10911919del, NC_000006.12:g.10911908_10911919del, NC_000006.12:g.10911909_10911919del, NC_000006.12:g.10911910_10911919del, NC_000006.12:g.10911911_10911919del, NC_000006.12:g.10911912_10911919del, NC_000006.12:g.10911913_10911919del, NC_000006.12:g.10911914_10911919del, NC_000006.12:g.10911915_10911919del, NC_000006.12:g.10911916_10911919del, NC_000006.12:g.10911917_10911919del, NC_000006.12:g.10911918_10911919del, NC_000006.12:g.10911919del, NC_000006.12:g.10911919dup, NC_000006.12:g.10911918_10911919dup, NC_000006.12:g.10911917_10911919dup, NC_000006.12:g.10911916_10911919dup, NC_000006.12:g.10911915_10911919dup, NC_000006.12:g.10911914_10911919dup, NC_000006.12:g.10911913_10911919dup, NC_000006.12:g.10911912_10911919dup, NC_000006.12:g.10911909_10911919dup, NC_000006.12:g.10911908_10911919dup, NC_000006.12:g.10911905_10911919dup, NC_000006.12:g.10911904_10911919dup, NC_000006.12:g.10911903_10911919dup, NC_000006.12:g.10911901_10911919dup, NC_000006.12:g.10911900_10911919dup, NC_000006.12:g.10911899_10911919dup, NC_000006.12:g.10911898_10911919dup, NC_000006.12:g.10911897_10911919dup, NC_000006.12:g.10911896_10911919dup, NC_000006.12:g.10911895_10911919dup, NC_000006.12:g.10911919_10911920insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10911919_10911920insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10911919_10911920insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10911919_10911920insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10912137_10912152del, NC_000006.11:g.10912139_10912152del, NC_000006.11:g.10912140_10912152del, NC_000006.11:g.10912141_10912152del, NC_000006.11:g.10912142_10912152del, NC_000006.11:g.10912143_10912152del, NC_000006.11:g.10912144_10912152del, NC_000006.11:g.10912145_10912152del, NC_000006.11:g.10912146_10912152del, NC_000006.11:g.10912147_10912152del, NC_000006.11:g.10912148_10912152del, NC_000006.11:g.10912149_10912152del, NC_000006.11:g.10912150_10912152del, NC_000006.11:g.10912151_10912152del, NC_000006.11:g.10912152del, NC_000006.11:g.10912152dup, NC_000006.11:g.10912151_10912152dup, NC_000006.11:g.10912150_10912152dup, NC_000006.11:g.10912149_10912152dup, NC_000006.11:g.10912148_10912152dup, NC_000006.11:g.10912147_10912152dup, NC_000006.11:g.10912146_10912152dup, NC_000006.11:g.10912145_10912152dup, NC_000006.11:g.10912142_10912152dup, NC_000006.11:g.10912141_10912152dup, NC_000006.11:g.10912138_10912152dup, NC_000006.11:g.10912137_10912152dup, NC_000006.11:g.10912136_10912152dup, NC_000006.11:g.10912134_10912152dup, NC_000006.11:g.10912133_10912152dup, NC_000006.11:g.10912132_10912152dup, NC_000006.11:g.10912131_10912152dup, NC_000006.11:g.10912130_10912152dup, NC_000006.11:g.10912129_10912152dup, NC_000006.11:g.10912128_10912152dup, NC_000006.11:g.10912152_10912153insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10912152_10912153insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10912152_10912153insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10912152_10912153insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
5.
rs1491533511 has merged into rs34095541 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTT>-,T,TT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTGTTTGGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:10914749
(GRCh38)
6:10914982
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTGGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10914738:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
T=0.1957/980
(1000Genomes)
- HGVS:
NC_000006.12:g.10914749_10914759del, NC_000006.12:g.10914750_10914759del, NC_000006.12:g.10914751_10914759del, NC_000006.12:g.10914755_10914759del, NC_000006.12:g.10914756_10914759del, NC_000006.12:g.10914757_10914759del, NC_000006.12:g.10914758_10914759del, NC_000006.12:g.10914759del, NC_000006.12:g.10914759dup, NC_000006.12:g.10914758_10914759dup, NC_000006.12:g.10914757_10914759dup, NC_000006.12:g.10914756_10914759dup, NC_000006.12:g.10914755_10914759dup, NC_000006.12:g.10914754_10914759dup, NC_000006.12:g.10914752_10914759dup, NC_000006.12:g.10914739_10914759T[29]GTTTGGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.10914759_10914760insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10914982_10914992del, NC_000006.11:g.10914983_10914992del, NC_000006.11:g.10914984_10914992del, NC_000006.11:g.10914988_10914992del, NC_000006.11:g.10914989_10914992del, NC_000006.11:g.10914990_10914992del, NC_000006.11:g.10914991_10914992del, NC_000006.11:g.10914992del, NC_000006.11:g.10914992dup, NC_000006.11:g.10914991_10914992dup, NC_000006.11:g.10914990_10914992dup, NC_000006.11:g.10914989_10914992dup, NC_000006.11:g.10914988_10914992dup, NC_000006.11:g.10914987_10914992dup, NC_000006.11:g.10914985_10914992dup, NC_000006.11:g.10914972_10914992T[29]GTTTGGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.10914992_10914993insTTTTTTTTTTTTTTTTTTTTTTTTTT
6.
rs1491500314 has merged into rs34273350 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTT>-,T,TT,TTTT,TTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:10889625
(GRCh38)
6:10889858
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10889616:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTT=0./0
(
ALFA)
-=0.36562/1831
(1000Genomes)
- HGVS:
NC_000006.12:g.10889625_10889637del, NC_000006.12:g.10889626_10889637del, NC_000006.12:g.10889627_10889637del, NC_000006.12:g.10889629_10889637del, NC_000006.12:g.10889630_10889637del, NC_000006.12:g.10889633_10889637del, NC_000006.12:g.10889634_10889637del, NC_000006.12:g.10889635_10889637del, NC_000006.12:g.10889636_10889637del, NC_000006.12:g.10889637del, NC_000006.12:g.10889637dup, NC_000006.12:g.10889636_10889637dup, NC_000006.12:g.10889635_10889637dup, NC_000006.12:g.10889634_10889637dup, NC_000006.12:g.10889633_10889637dup, NC_000006.12:g.10889632_10889637dup, NC_000006.12:g.10889631_10889637dup, NC_000006.12:g.10889625_10889637dup, NC_000006.12:g.10889620_10889637dup, NC_000006.12:g.10889619_10889637dup, NC_000006.12:g.10889637_10889638insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10889858_10889870del, NC_000006.11:g.10889859_10889870del, NC_000006.11:g.10889860_10889870del, NC_000006.11:g.10889862_10889870del, NC_000006.11:g.10889863_10889870del, NC_000006.11:g.10889866_10889870del, NC_000006.11:g.10889867_10889870del, NC_000006.11:g.10889868_10889870del, NC_000006.11:g.10889869_10889870del, NC_000006.11:g.10889870del, NC_000006.11:g.10889870dup, NC_000006.11:g.10889869_10889870dup, NC_000006.11:g.10889868_10889870dup, NC_000006.11:g.10889867_10889870dup, NC_000006.11:g.10889866_10889870dup, NC_000006.11:g.10889865_10889870dup, NC_000006.11:g.10889864_10889870dup, NC_000006.11:g.10889858_10889870dup, NC_000006.11:g.10889853_10889870dup, NC_000006.11:g.10889852_10889870dup, NC_000006.11:g.10889870_10889871insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
7.
rs1491497048 has merged into rs201059528 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAA>-,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 6:10959873
(GRCh38)
6:10960106
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:10959869:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAA=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
A=0.260583/1305
(1000Genomes)
- HGVS:
NC_000006.12:g.10959873_10959884del, NC_000006.12:g.10959880_10959884del, NC_000006.12:g.10959881_10959884del, NC_000006.12:g.10959882_10959884del, NC_000006.12:g.10959883_10959884del, NC_000006.12:g.10959884del, NC_000006.12:g.10959884dup, NC_000006.12:g.10959883_10959884dup, NC_000006.12:g.10959882_10959884dup, NC_000006.12:g.10959881_10959884dup, NC_000006.12:g.10959880_10959884dup, NC_000006.12:g.10959878_10959884dup, NC_000006.11:g.10960106_10960117del, NC_000006.11:g.10960113_10960117del, NC_000006.11:g.10960114_10960117del, NC_000006.11:g.10960115_10960117del, NC_000006.11:g.10960116_10960117del, NC_000006.11:g.10960117del, NC_000006.11:g.10960117dup, NC_000006.11:g.10960116_10960117dup, NC_000006.11:g.10960115_10960117dup, NC_000006.11:g.10960114_10960117dup, NC_000006.11:g.10960113_10960117dup, NC_000006.11:g.10960111_10960117dup
9.
rs1491452988 has merged into rs3066124 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GTGTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
[Show Flanks]
- Chromosome:
- 6:10891643
(GRCh38)
6:10891876
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10891613:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0./0
(
ALFA)
- HGVS:
NC_000006.12:g.10891615GT[14], NC_000006.12:g.10891615GT[15], NC_000006.12:g.10891615GT[16], NC_000006.12:g.10891615GT[17], NC_000006.12:g.10891615GT[18], NC_000006.12:g.10891615GT[19], NC_000006.12:g.10891615GT[20], NC_000006.12:g.10891615GT[21], NC_000006.12:g.10891615GT[22], NC_000006.12:g.10891615GT[23], NC_000006.12:g.10891615GT[24], NC_000006.12:g.10891615GT[26], NC_000006.12:g.10891615GT[27], NC_000006.12:g.10891615GT[28], NC_000006.12:g.10891615GT[29], NC_000006.12:g.10891615GT[30], NC_000006.11:g.10891848GT[14], NC_000006.11:g.10891848GT[15], NC_000006.11:g.10891848GT[16], NC_000006.11:g.10891848GT[17], NC_000006.11:g.10891848GT[18], NC_000006.11:g.10891848GT[19], NC_000006.11:g.10891848GT[20], NC_000006.11:g.10891848GT[21], NC_000006.11:g.10891848GT[22], NC_000006.11:g.10891848GT[23], NC_000006.11:g.10891848GT[24], NC_000006.11:g.10891848GT[26], NC_000006.11:g.10891848GT[27], NC_000006.11:g.10891848GT[28], NC_000006.11:g.10891848GT[29], NC_000006.11:g.10891848GT[30]
11.
rs1491363803 has merged into rs551103839 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:10907902
(GRCh38)
6:10908135
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10907892:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
-=0.0437/219
(1000Genomes)
- HGVS:
NC_000006.12:g.10907902_10907910del, NC_000006.12:g.10907903_10907910del, NC_000006.12:g.10907905_10907910del, NC_000006.12:g.10907906_10907910del, NC_000006.12:g.10907907_10907910del, NC_000006.12:g.10907908_10907910del, NC_000006.12:g.10907909_10907910del, NC_000006.12:g.10907910del, NC_000006.12:g.10907910dup, NC_000006.12:g.10907909_10907910dup, NC_000006.12:g.10907908_10907910dup, NC_000006.12:g.10907907_10907910dup, NC_000006.12:g.10907906_10907910dup, NC_000006.12:g.10907905_10907910dup, NC_000006.12:g.10907904_10907910dup, NC_000006.12:g.10907903_10907910dup, NC_000006.12:g.10907902_10907910dup, NC_000006.12:g.10907901_10907910dup, NC_000006.12:g.10907900_10907910dup, NC_000006.12:g.10907899_10907910dup, NC_000006.12:g.10907898_10907910dup, NC_000006.12:g.10907897_10907910dup, NC_000006.12:g.10907896_10907910dup, NC_000006.12:g.10907895_10907910dup, NC_000006.12:g.10907894_10907910dup, NC_000006.12:g.10907893_10907910dup, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907893_10907910T[58]CTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.10907910_10907911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908135_10908143del, NC_000006.11:g.10908136_10908143del, NC_000006.11:g.10908138_10908143del, NC_000006.11:g.10908139_10908143del, NC_000006.11:g.10908140_10908143del, NC_000006.11:g.10908141_10908143del, NC_000006.11:g.10908142_10908143del, NC_000006.11:g.10908143del, NC_000006.11:g.10908143dup, NC_000006.11:g.10908142_10908143dup, NC_000006.11:g.10908141_10908143dup, NC_000006.11:g.10908140_10908143dup, NC_000006.11:g.10908139_10908143dup, NC_000006.11:g.10908138_10908143dup, NC_000006.11:g.10908137_10908143dup, NC_000006.11:g.10908136_10908143dup, NC_000006.11:g.10908135_10908143dup, NC_000006.11:g.10908134_10908143dup, NC_000006.11:g.10908133_10908143dup, NC_000006.11:g.10908132_10908143dup, NC_000006.11:g.10908131_10908143dup, NC_000006.11:g.10908130_10908143dup, NC_000006.11:g.10908129_10908143dup, NC_000006.11:g.10908128_10908143dup, NC_000006.11:g.10908127_10908143dup, NC_000006.11:g.10908126_10908143dup, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908126_10908143T[58]CTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.10908143_10908144insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
15.
rs1491232016 has merged into rs5874297 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AA>-,A,AAA,AAAA,AAAAA,AAAAAAA
[Show Flanks]
- Chromosome:
- 6:10952596
(GRCh38)
6:10952829
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10952584:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:10952584:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:10952584:AAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:10952584:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:10952584:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:10952584:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA
- Gene:
- SYCP2L (Varview), LOC101928191 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAA=0./0
(
ALFA)
-=0.0065/25
(ALSPAC)
-=0.01/37
(TWINSUK)
-=0.125/5
(GENOME_DK)
-=0.1955/979
(1000Genomes)
- HGVS:
NC_000006.12:g.10952596_10952597del, NC_000006.12:g.10952597del, NC_000006.12:g.10952597dup, NC_000006.12:g.10952596_10952597dup, NC_000006.12:g.10952595_10952597dup, NC_000006.12:g.10952593_10952597dup, NC_000006.11:g.10952829_10952830del, NC_000006.11:g.10952830del, NC_000006.11:g.10952830dup, NC_000006.11:g.10952829_10952830dup, NC_000006.11:g.10952828_10952830dup, NC_000006.11:g.10952826_10952830dup
17.
rs1491169591 has merged into rs3066151 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GTGTGTGTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
[Show Flanks]
- Chromosome:
- 6:10967471
(GRCh38)
6:10967704
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000006.12:10967454:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GTGTGTGTGTGTGTGT=0./0
(
ALFA)
GT=0.05327/887
(TOMMO)
- HGVS:
NC_000006.12:g.10967455GT[8], NC_000006.12:g.10967455GT[9], NC_000006.12:g.10967455GT[10], NC_000006.12:g.10967455GT[11], NC_000006.12:g.10967455GT[12], NC_000006.12:g.10967455GT[13], NC_000006.12:g.10967455GT[14], NC_000006.12:g.10967455GT[15], NC_000006.12:g.10967455GT[16], NC_000006.12:g.10967455GT[17], NC_000006.12:g.10967455GT[18], NC_000006.12:g.10967455GT[19], NC_000006.12:g.10967455GT[20], NC_000006.12:g.10967455GT[22], NC_000006.12:g.10967455GT[23], NC_000006.12:g.10967455GT[24], NC_000006.12:g.10967455GT[25], NC_000006.12:g.10967455GT[26], NC_000006.12:g.10967455GT[27], NC_000006.12:g.10967455GT[28], NC_000006.12:g.10967455GT[29], NC_000006.12:g.10967455GT[30], NC_000006.12:g.10967455GT[31], NC_000006.12:g.10967455GT[32], NC_000006.11:g.10967688GT[8], NC_000006.11:g.10967688GT[9], NC_000006.11:g.10967688GT[10], NC_000006.11:g.10967688GT[11], NC_000006.11:g.10967688GT[12], NC_000006.11:g.10967688GT[13], NC_000006.11:g.10967688GT[14], NC_000006.11:g.10967688GT[15], NC_000006.11:g.10967688GT[16], NC_000006.11:g.10967688GT[17], NC_000006.11:g.10967688GT[18], NC_000006.11:g.10967688GT[19], NC_000006.11:g.10967688GT[20], NC_000006.11:g.10967688GT[22], NC_000006.11:g.10967688GT[23], NC_000006.11:g.10967688GT[24], NC_000006.11:g.10967688GT[25], NC_000006.11:g.10967688GT[26], NC_000006.11:g.10967688GT[27], NC_000006.11:g.10967688GT[28], NC_000006.11:g.10967688GT[29], NC_000006.11:g.10967688GT[30], NC_000006.11:g.10967688GT[31], NC_000006.11:g.10967688GT[32]
19.
rs1491143215 has merged into rs34659978 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 6:10905156
(GRCh38)
6:10905389
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:10905142:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAAA=0./0
(
ALFA)
- HGVS:
NC_000006.12:g.10905156_10905166del, NC_000006.12:g.10905157_10905166del, NC_000006.12:g.10905158_10905166del, NC_000006.12:g.10905159_10905166del, NC_000006.12:g.10905160_10905166del, NC_000006.12:g.10905161_10905166del, NC_000006.12:g.10905162_10905166del, NC_000006.12:g.10905163_10905166del, NC_000006.12:g.10905164_10905166del, NC_000006.12:g.10905165_10905166del, NC_000006.12:g.10905166del, NC_000006.12:g.10905166dup, NC_000006.12:g.10905165_10905166dup, NC_000006.12:g.10905164_10905166dup, NC_000006.12:g.10905163_10905166dup, NC_000006.12:g.10905162_10905166dup, NC_000006.12:g.10905161_10905166dup, NC_000006.12:g.10905160_10905166dup, NC_000006.12:g.10905159_10905166dup, NC_000006.12:g.10905158_10905166dup, NC_000006.12:g.10905157_10905166dup, NC_000006.12:g.10905156_10905166dup, NC_000006.12:g.10905155_10905166dup, NC_000006.12:g.10905154_10905166dup, NC_000006.12:g.10905153_10905166dup, NC_000006.12:g.10905152_10905166dup, NC_000006.12:g.10905151_10905166dup, NC_000006.12:g.10905149_10905166dup, NC_000006.11:g.10905389_10905399del, NC_000006.11:g.10905390_10905399del, NC_000006.11:g.10905391_10905399del, NC_000006.11:g.10905392_10905399del, NC_000006.11:g.10905393_10905399del, NC_000006.11:g.10905394_10905399del, NC_000006.11:g.10905395_10905399del, NC_000006.11:g.10905396_10905399del, NC_000006.11:g.10905397_10905399del, NC_000006.11:g.10905398_10905399del, NC_000006.11:g.10905399del, NC_000006.11:g.10905399dup, NC_000006.11:g.10905398_10905399dup, NC_000006.11:g.10905397_10905399dup, NC_000006.11:g.10905396_10905399dup, NC_000006.11:g.10905395_10905399dup, NC_000006.11:g.10905394_10905399dup, NC_000006.11:g.10905393_10905399dup, NC_000006.11:g.10905392_10905399dup, NC_000006.11:g.10905391_10905399dup, NC_000006.11:g.10905390_10905399dup, NC_000006.11:g.10905389_10905399dup, NC_000006.11:g.10905388_10905399dup, NC_000006.11:g.10905387_10905399dup, NC_000006.11:g.10905386_10905399dup, NC_000006.11:g.10905385_10905399dup, NC_000006.11:g.10905384_10905399dup, NC_000006.11:g.10905382_10905399dup
20.
rs1491118544 has merged into rs149829365 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:10963974
(GRCh38)
6:10964207
(GRCh37)
- Canonical SPDI:
- NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:10963961:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- SYCP2L (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTTT=0./0
(
ALFA)
T=0.3217/1611
(1000Genomes)
- HGVS:
NC_000006.12:g.10963974_10963977del, NC_000006.12:g.10963975_10963977del, NC_000006.12:g.10963976_10963977del, NC_000006.12:g.10963977del, NC_000006.12:g.10963977dup, NC_000006.12:g.10963976_10963977dup, NC_000006.12:g.10963975_10963977dup, NC_000006.12:g.10963973_10963977dup, NC_000006.12:g.10963964_10963977dup, NC_000006.11:g.10964207_10964210del, NC_000006.11:g.10964208_10964210del, NC_000006.11:g.10964209_10964210del, NC_000006.11:g.10964210del, NC_000006.11:g.10964210dup, NC_000006.11:g.10964209_10964210dup, NC_000006.11:g.10964208_10964210dup, NC_000006.11:g.10964206_10964210dup, NC_000006.11:g.10964197_10964210dup