89575787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 123844165-G-A

89575787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 123844165-G-C

89575787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 123844165-G-T

89575839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 123844210-G-A

89575839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 123844210-G-T

89575925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 123844263-G-A

89575925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 123844263-G-C

89575925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 123844263-G-T

http://identifiers.org/hco/16/GRCh38#89576032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#123844364-C-A

89576032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 123844364-C-G

89576032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 123844364-C-T

89576108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123844419-G-A

89576108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123844419-G-T

89576152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123844451-G-A

89576152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123844451-G-C

89576152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123844451-G-T

89576281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123844556-T-G

89576355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123844617-G-T

89577100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123845856-G-A

89577192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123845920-C-T

89577222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123845952-G-A

http://identifiers.org/hco/16/GRCh38#89577420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123846174-C-A

89577420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846174-C-G

89577420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846174-C-T

89577474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846279-G-A

89577474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846279-G-T

89577525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: 123846343-A-G

89577631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123846450-G-T

89577785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846586-G-T

http://identifiers.org/hco/16/GRCh38#89577786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123846587-C-A

89577857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846646-G-T

89577863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846650-T-A

89577863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846650-T-C

89578067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846780-C-T

89578214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846874-G-A

89578245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846913-A-T

89578257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123846935-G-A

89578305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123847005-C-T

89578352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123847051-G-A

89578359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123847058-A-G

89578359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123847058-A-T

89578398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123847093-G-A

89583655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123850841-G-A

89583655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123850841-G-T

89583656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123850842-T-C

89583705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123850895-C-G

89583705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123850895-C-T

http://identifiers.org/hco/16/GRCh38#89583721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123850911-C-A

89583721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: missense variant
orthologous variants: 123850911-C-T

89583726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: synonymous variant
orthologous variants: 123850916-G-A

89583726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: synonymous variant
orthologous variants: 123850916-G-C

89583726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: synonymous variant
orthologous variants: 123850916-G-T

http://identifiers.org/hco/16/GRCh38#89583736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123850926-A-C

89583846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851004-G-T

http://identifiers.org/hco/16/GRCh38#89583852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123851010-C-A

89583852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851010-C-T

89583901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851046-C-G

89583901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851046-C-T

http://identifiers.org/hco/16/GRCh38#89583949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123851080-C-A

89583949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851080-C-G

89583949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851080-C-T

http://identifiers.org/hco/16/GRCh38#89583953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123851084-C-A

89583953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851084-C-G

89583953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851084-C-T

89583993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851106-T-C

http://identifiers.org/hco/16/GRCh38#89584156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123851269-C-A

89584156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron variant
orthologous variants: 123851269-C-T

http://identifiers.org/hco/16/GRCh38#89584768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123852295-C-A

http://identifiers.org/hco/16/GRCh38#89584791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123852318-C-A

89584791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: synonymous variant
orthologous variants: 123852318-C-G

89584791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: synonymous variant
orthologous variants: 123852318-C-T

89584818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: synonymous variant
orthologous variants: 123852345-C-G

89584863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852398-C-G

89584863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852398-C-T

89584864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123852399-G-A

89584864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123852399-G-T

89584865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123852400-G-T

89584873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852411-T-C

89584873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852411-T-G

89584944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852489-G-C

http://identifiers.org/hco/16/GRCh38#89584952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123852497-C-A

89584952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852497-C-T

89585180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852705-A-G

http://identifiers.org/hco/16/GRCh38#89585316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123852833-C-A

89585320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852837-T-C

89585401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123852917-C-G

89585499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123853015-C-T

89585532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123853048-C-G

89585532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123853048-C-T

89585566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853083-A-T

89585593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853126-G-A

89585593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853126-G-T

89585598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853131-G-T

89585601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853134-G-A

89585602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853157-T-G

89585611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853169-A-G

89585611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853169-A-T

http://identifiers.org/hco/16/GRCh38#89585619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123853193-A-C

89585620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853194-C-G

89585623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853197-G-A

89585623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853197-G-C

89585646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853329-G-A

89585646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853329-G-C

89585664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853350-C-T

http://identifiers.org/hco/16/GRCh38#89585681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123853366-C-A

89585681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123853366-C-T

http://identifiers.org/hco/16/GRCh38#89585770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123853455-C-A

89586224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853581-C-T

89586392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853725-G-T

89586397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853730-C-T

89586398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853731-C-T

89586423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853747-G-A

89586541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853911-A-T

89586558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853928-T-A

89586558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853928-T-C

89586602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853973-G-A

89586602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123853973-G-T

89586643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854059-G-T

89586662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123854084-T-C

89586733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123854155-G-C

89586817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854230-C-G

89586817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854230-C-T

89586850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854271-G-A

89586850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854271-G-T

89587014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854421-G-A

89587014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854421-G-C

89587014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854421-G-T

89587112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854542-T-C

89587112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854542-T-G

89587137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854570-A-G

89587138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854571-G-A

89587138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854571-G-T

89587150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854583-G-A

89587150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854583-G-C

89587150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854583-G-T

89587155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123854588-G-A

89587155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123854588-G-C

89587155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123854588-G-T

89587156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123854589-C-G

89587156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123854589-C-T

http://identifiers.org/hco/16/GRCh38#89587493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123854718-C-A

89587493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123854718-C-T

89587555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 123854794-G-A

89587555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 123854794-G-C

89587556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 123854795-A-G

89587556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 123854795-A-T

89587563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123854802-G-A

89587563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123854802-G-C

http://identifiers.org/hco/16/GRCh38#89587601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123854856-C-A

89587601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123854856-C-T

http://identifiers.org/hco/16/GRCh38#89587642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123854906-A-C

89588656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 123855298-G-A

89588656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 123855298-G-C

89588665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 123855307-C-T

89588819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123855461-C-T

89589960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856345-G-A

89589960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856345-G-C

89589960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856345-G-T

89590036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856416-T-G

89590062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856433-G-A

89590062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856433-G-T

89590066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856438-G-A

89590067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856439-A-G

89590073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856445-T-C

89590085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856454-G-A

89590085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123856454-G-T

89591015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 123856801-T-A

89591015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 123856801-T-G

89591143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 123856928-G-A

89591173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 123856958-C-G

89591173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 123856958-C-T

http://identifiers.org/hco/16/GRCh38#89591182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#123856967-C-A

89591182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 123856967-C-T

http://identifiers.org/hco/16/GRCh38#89591203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123856988-C-A

89591203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 123856988-C-T

89591233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 123857018-G-A

89591299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857076-G-A

89591299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857076-G-C

89591299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857076-G-T

89591328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857111-G-A

89591328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857111-G-T

http://identifiers.org/hco/16/GRCh38#89591348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123857131-A-C

89591348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857131-A-G

89591348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857131-A-T

http://identifiers.org/hco/16/GRCh38#89591372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123857153-C-A

89591372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857153-C-G

89591372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857153-C-T

89591376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857157-G-A

89591376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857157-G-T

http://identifiers.org/hco/16/GRCh38#89591377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123857158-C-A

89591377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857158-C-T

89591379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857160-G-A

89591379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857160-G-T

89591383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857164-A-G

89591398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857181-G-A

89591398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857181-G-T

89591445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123857240-C-T

89591451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123857246-C-G

89591464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123857261-C-G

89591464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123857261-C-T

89591465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123857262-G-A

89591465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123857262-G-T

89591487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123857281-G-C

89591689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123857445-G-A

89595405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123860386-G-A

89595405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123860386-G-C

89595405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123860386-G-T

89595407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123860388-C-T

89595477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123860458-C-G

89595477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123860458-C-T

89595516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123860497-C-T

http://identifiers.org/hco/16/GRCh38#89595532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123860513-C-A

89595532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123860513-C-T

89595643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123860636-G-T

89595651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123860644-T-A

89595651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123860644-T-G

89595684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123860672-G-A

89595684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123860672-G-T

89595727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123860703-G-A

89595727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123860703-G-T

89595728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123860704-A-G

http://identifiers.org/hco/16/GRCh38#89595815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123860757-C-A

89595815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123860757-C-G

89595815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123860757-C-T

89595817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123860759-A-T

89596582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123861277-T-A

89596582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123861277-T-C

89596582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123861277-T-G

89596650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861331-T-C

89596659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861340-G-A

89596659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861340-G-C

89596659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861340-G-T

http://identifiers.org/hco/16/GRCh38#89596663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123861344-C-A

89596663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861344-C-T

89596768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861438-T-A

89596768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861438-T-C

89596773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861448-G-A

89596773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861448-G-C

89596773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861448-G-T

http://identifiers.org/hco/16/GRCh38#89596794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123861469-C-A

89596815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123861492-A-T

89596831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123861512-G-A

89596844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123861525-T-A

89596844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123861525-T-C

http://identifiers.org/hco/16/GRCh38#89596870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123861551-A-C

89596870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: 123861551-A-G

89596870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: 123861551-A-T

89596882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: 123861563-T-A

http://identifiers.org/hco/16/GRCh38#89597104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123861844-C-A

89597104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: 123861844-C-T

http://identifiers.org/hco/16/GRCh38#89597157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123861864-A-C

89597157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: 123861864-A-G

http://identifiers.org/hco/16/GRCh38#89597167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123861874-C-A

89597167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2320
most severe consequence: 3 prime UTR variant
orthologous variants: 123861874-C-T