http://identifiers.org/hco/13/GRCh38#43023793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#78112176-C-A

43023793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78112176-C-G

43023793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78112176-C-T

http://identifiers.org/hco/13/GRCh38#43023796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78112173-C-A

43023796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78112173-C-G

43023859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78112102-G-A

43023859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78112102-G-T

43026006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78111482-C-T

43026349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78111073-C-T

43026473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78110947-G-A

43027081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78110292-T-C

43028023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109475-G-A

43028069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109447-T-G

43028070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109446-G-A

43028293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109400-C-G

43028293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78109400-C-T

http://identifiers.org/hco/13/GRCh38#43028641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78109064-C-A

43028793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78108895-T-G

43029063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78108059-A-G

43029194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78107938-G-C

43029363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78107805-C-T

43038856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78105245-T-A

43039235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78105125-T-G

43039515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78104877-G-A

43039515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78104877-G-C

43041682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78103425-T-C

43043422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78102326-A-G

43043422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78102326-A-T

43043433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78102315-A-G

43043859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101972-A-G

43044050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101755-C-G

43044081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101701-C-G

43044081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101701-C-T

43044339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101461-G-T

43044394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101421-T-C

43044456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101361-C-T

43044463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101354-C-T

43044484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78101331-C-T

43050881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78099514-T-A

43062428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78098384-G-A

43062466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78098346-G-T

43063615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78096666-T-C

43064957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78095573-T-A

http://identifiers.org/hco/13/GRCh38#43064958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78095572-C-A

43065050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78095491-A-G

43065051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78095490-T-A

43065051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78095490-T-C

43065087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78095454-T-C

43065159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78095374-G-A

43065159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78095374-G-C

http://identifiers.org/hco/13/GRCh38#43065297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78095233-C-A

43065525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78094581-A-G

43065592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78094516-G-A

43065592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78094516-G-T

43065850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78094349-T-A

43065850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78094349-T-C

43065880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78094326-T-G

43066851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78093095-C-T

43066914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78093033-C-T

43067016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78092973-G-A

43067016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78092973-G-T

43067087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78092526-A-G

43067087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78092526-A-T

43067344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78092328-T-A

43067425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78092251-A-G

43067752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78091947-G-A

43067882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78091818-T-C

43068335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78091067-C-T

43068476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78090904-A-G

43068968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78090371-G-C

43068968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78090371-G-T

43069104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78090237-T-C

http://identifiers.org/hco/13/GRCh38#43069196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78090150-C-A

43069692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78089089-T-A

43070217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78088958-T-G

http://identifiers.org/hco/13/GRCh38#43070312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78088865-A-C

43070320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78088857-A-G

43071006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78088185-A-G

http://identifiers.org/hco/13/GRCh38#43071314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78087919-C-A

43071314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78087919-C-T

43071343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78087915-G-A

http://identifiers.org/hco/13/GRCh38#43071541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78087777-C-A

43071717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78087619-A-T

43071730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78087606-A-G

43071766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78087582-G-A

43071766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78087582-G-T

43071846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78087504-A-G

43071952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78087398-G-T

43071979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78087372-G-A

43072045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78087312-G-A

43073916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78085824-A-G

43074410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78085466-A-G

43074715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78085174-T-C

43074887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78085051-A-G

43075056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78085017-T-C

43075647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78084596-A-G

43075693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78084560-G-A

43076658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78084023-G-A

http://identifiers.org/hco/13/GRCh38#43076992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78083547-C-A

43077022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78083517-C-T

43077295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78083270-T-C

43077576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78083024-A-G

43078233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78082435-G-A

43078334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78082336-A-G

http://identifiers.org/hco/13/GRCh38#43078569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78081949-A-C

43078744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78081774-A-G

http://identifiers.org/hco/13/GRCh38#43078833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78081682-C-A

43078833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78081682-C-T

43078902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78081658-G-C

43078902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78081658-G-T

43079037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78081531-C-T

43082553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78080299-T-A

43082559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78080293-G-A

43082583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78080275-T-C

43082637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78080214-C-T

43083578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78079666-G-A

43083850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78079423-C-T

http://identifiers.org/hco/13/GRCh38#43083859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78079413-C-A

43084075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78079049-T-C

43084086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78079039-G-A

43084132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78078994-C-T

43084411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78078770-T-C

43084441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78078742-G-A

43084445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78078738-T-G

43084475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78078707-T-C

43084785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78078428-T-G

43084899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78078319-T-A

43085783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: missense variant
orthologous variants: 78077661-G-T

43085817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: missense variant
orthologous variants: 78077627-A-G

43085957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077471-G-T

43085985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077441-G-A

43085985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077441-G-C

43085985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077441-G-T

43086069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077358-C-T

43086119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077313-G-A

43086127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077305-G-A

43086243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077192-G-C

43086286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78077149-C-G

http://identifiers.org/hco/13/GRCh38#43086533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78076909-C-A

43086662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78076783-G-A

43086793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78076652-G-T

43087421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78075875-A-G

43087585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78075741-T-G

43093825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78075379-A-G

43093874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78075342-G-A

43094067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78075169-T-C

43094641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78074696-A-G

43094693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78074648-G-A

43095165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78074186-G-A

43095492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78073892-C-T

http://identifiers.org/hco/13/GRCh38#43095557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78073746-C-A

43095599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78073645-C-T

43095601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78073643-C-T

43095766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78073420-A-T

43095859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78073264-G-C

43096092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78073026-C-T

43096301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78072814-G-A

43105440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78065906-G-A

43105450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78065896-G-A

43105450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78065896-G-C

43105915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78065064-A-T

43106018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78064962-G-C

43106054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78064938-T-A

43106054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78064938-T-C

43106100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78064893-G-T

43106171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78064823-T-C

43107041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: intron variant
orthologous variants: 78064041-T-C

43107282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063797-G-A

43107282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063797-G-T

http://identifiers.org/hco/13/GRCh38#43107518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78063587-C-A

43107518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063587-C-G

http://identifiers.org/hco/13/GRCh38#43107564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78063563-A-C

43107564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063563-A-G

43107628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063497-G-A

http://identifiers.org/hco/13/GRCh38#43107819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78063314-C-A

43107819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063314-C-T

43107858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063275-G-T

http://identifiers.org/hco/13/GRCh38#43107863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78063270-A-C

43107863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063270-A-G

43107941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063184-T-C

43107941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78063184-T-G

43108311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062809-T-C

43108326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062794-G-T

http://identifiers.org/hco/13/GRCh38#43109556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78062721-C-A

43109587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062688-G-A

43109725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062576-G-A

43109725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062576-G-C

43109725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062576-G-T

43109899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062566-G-T

43109972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062503-G-A

43110087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062395-G-T

http://identifiers.org/hco/13/GRCh38#43110107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78062376-C-A

43110127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062355-G-A

43110163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062319-G-A

43110164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062318-T-C

http://identifiers.org/hco/13/GRCh38#43110238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78062262-C-A

43110253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062246-A-G

43110346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78062182-T-C

http://identifiers.org/hco/13/GRCh38#43110502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78062092-C-A

43110831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061777-C-T

http://identifiers.org/hco/13/GRCh38#43110857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78061754-C-A

43110857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061754-C-G

http://identifiers.org/hco/13/GRCh38#43110982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78061635-A-C

43111119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061492-G-A

43111127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061484-C-G

43111127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061484-C-T

43111173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061438-G-C

43111179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061432-A-G

43111215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061389-A-G

43111331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061274-A-G

43111621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78061024-A-G

http://identifiers.org/hco/13/GRCh38#43111687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78060958-C-A

43111794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060850-G-A

43111794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060850-G-T

43111965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060683-T-A

43112014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060634-G-A

43112047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060589-C-T

43112115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060529-T-G

http://identifiers.org/hco/13/GRCh38#43112252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78060411-C-A

43112252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060411-C-T

http://identifiers.org/hco/13/GRCh38#43112253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78060410-C-A

43112253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060410-C-T

43112288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060376-G-A

43112288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060376-G-T

http://identifiers.org/hco/13/GRCh38#43112296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#78060368-C-A

43112296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060368-C-T

43112517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78060104-G-T

43112884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78059782-C-T

43112909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78059755-G-T

43113039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78059649-G-A

43113107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3 prime UTR variant
orthologous variants: 78059578-A-G

43113473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78059071-A-G

43113573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058758-G-T

43113672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058633-A-G

43113778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058509-G-T

43113796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058492-G-A

43113796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058492-G-T

43113829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058462-G-T

43113916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058377-G-A

43114108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058226-T-A

43114146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78058187-A-T