http://identifiers.org/hco/16/GRCh38#88570471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#123103445-C-A

88570471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 123103445-C-G

88570471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 123103445-C-T

88570563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 123103536-T-C

88570578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, undefined
orthologous variants: 123103549-C-T

88570588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123103559-G-A

88570588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123103559-G-T

88570880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, undefined
orthologous variants: 123103796-C-T

88570950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, undefined
orthologous variants: 123103863-C-T

88571326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123104233-A-G

88571509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123104342-G-A

http://identifiers.org/hco/16/GRCh38#88571668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123104485-A-C

88571668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123104485-A-T

http://identifiers.org/hco/16/GRCh38#88571793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#123104596-C-A

88572893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123105776-G-A

88572893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123105776-G-T

88572903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123105786-A-T

88572904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123105787-C-G

88572904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123105787-C-T

88573129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123107499-A-G

88573273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123107659-C-T

http://identifiers.org/hco/16/GRCh38#88573293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123107679-C-A

88575056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123108833-C-G

88575121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123108904-G-A

88575121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123108904-G-C

88575592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123109483-G-A

88576745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123109894-A-T

http://identifiers.org/hco/16/GRCh38#88576747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123109896-A-C

88576747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123109896-A-G

88576749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123109898-T-C

88576785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123109934-G-A

http://identifiers.org/hco/16/GRCh38#88576845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123109985-C-A

88576991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123110054-G-T

http://identifiers.org/hco/16/GRCh38#88577087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123110116-A-C

88577087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123110116-A-G

88577087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123110116-A-T

88577091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123110120-T-A

88577091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123110120-T-C

88577210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: synonymous variant
orthologous variants: 123110236-G-T

88577213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: missense variant
orthologous variants: 123110239-G-T

http://identifiers.org/hco/16/GRCh38#88577219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123110245-C-A

88577219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: synonymous variant
orthologous variants: 123110245-C-T

88577248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: missense variant
orthologous variants: 123110274-G-A

88577258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: synonymous variant
orthologous variants: 123110284-T-C

http://identifiers.org/hco/16/GRCh38#88577288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123110314-C-A

88577414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 123110434-C-T

88577545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant
orthologous variants: 123110562-C-G

88577545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant
orthologous variants: 123110562-C-T

88577558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant
orthologous variants: 123110575-C-G

88577558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 123110575-C-T

88577612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 123110629-C-T

88577622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant
orthologous variants: 123110639-G-A

88577670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant
orthologous variants: 123110687-G-A

88577726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 123110743-C-T

http://identifiers.org/hco/16/GRCh38#88577846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123110861-C-A

88578419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123111070-T-A

88578419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123111070-T-G

88578426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123111080-G-A

88579523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123111735-T-C

88579687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123111911-C-G

88579687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123111911-C-T

88586131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123113197-G-A

88586490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123113495-T-C

88586743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123113746-G-A

88586743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123113746-G-T

88586828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123113822-T-C

88586828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123113822-T-G

88587025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123113998-G-T

88587141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123114104-G-C

88587141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123114104-G-T

88587219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123114172-G-A

88587219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123114172-G-C

88587243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123114195-G-T

http://identifiers.org/hco/16/GRCh38#88587467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123114353-C-A

88587796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123114689-A-G

88588069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123114977-C-G

88588096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123115001-G-A

88588132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123115044-A-G

88588239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123115149-T-G

88588350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123115232-C-G

88588350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123115232-C-T

88588524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123115360-G-A

88588615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123115425-A-G

88588615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123115425-A-T

88594443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123122229-G-C

88594727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123122530-G-A

88598135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, undefined
orthologous variants: 123124514-A-G

88598135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, undefined
orthologous variants: 123124514-A-T

http://identifiers.org/hco/16/GRCh38#88598383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123124760-A-C

88598468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123124837-G-A

88598468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123124837-G-T

88598474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123124843-G-A

88598490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123124856-G-A

88598490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123124856-G-T

88598559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123124921-G-T

88598700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: synonymous variant
orthologous variants: 123125055-G-A

88598700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: synonymous variant
orthologous variants: 123125055-G-C

http://identifiers.org/hco/16/GRCh38#88598804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123125165-C-A

88598804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125165-C-T

http://identifiers.org/hco/16/GRCh38#88598806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123125167-C-A

88598806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125167-C-T

88598832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125185-G-A

88599105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125277-A-G

88599191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125326-G-C

88599194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125329-G-A

88599707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125662-G-A

88599707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125662-G-C

88599707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125662-G-T

http://identifiers.org/hco/16/GRCh38#88599761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123125713-A-C

88599761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125713-A-G

88599761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron variant
orthologous variants: 123125713-A-T

88599847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123125800-G-A

88599847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123125800-G-C

88599987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123125940-G-A

88599989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123125942-A-G

88599993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123125946-G-A

88608664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123128054-T-C

http://identifiers.org/hco/16/GRCh38#88608786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123128160-A-C

88608786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123128160-A-G

88608786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123128160-A-T

88608862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123128256-T-C

88608862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123128256-T-G

88609033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123128429-G-A

88610308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123129097-C-G

88610308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123129097-C-T

88610528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123129203-C-G

88610528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123129203-C-T

88610535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123129210-G-A

88610535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123129210-G-T

88610767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123129399-G-T

88610977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123129591-G-T

88611313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123129935-G-A

88611313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 123129935-G-T

88611510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123130132-C-G

88611510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123130132-C-T

88618786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123132245-T-G

88618846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123132295-G-A

http://identifiers.org/hco/16/GRCh38#88622548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123134385-C-A

88622548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134385-C-T

http://identifiers.org/hco/16/GRCh38#88622667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123134487-C-A

88622667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134487-C-T

88622678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134498-G-A

88622678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134498-G-T

88622859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134645-T-C

88622859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134645-T-G

88622861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134647-G-A

88622861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134647-G-T

88622949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134737-G-A

88622949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134737-G-T

http://identifiers.org/hco/16/GRCh38#88623002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123134780-A-C

88623055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134802-G-A

88623055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134802-G-C

88623055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123134802-G-T

88623225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123134988-T-C

88623381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123135137-T-C

88623381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123135137-T-G

88623393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123135149-G-C

88623393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123135149-G-T

88623419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123135174-G-A

88623904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137561-G-A

http://identifiers.org/hco/16/GRCh38#88623927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123137590-C-A

88623927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137590-C-G

88623927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137590-C-T

http://identifiers.org/hco/16/GRCh38#88624051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123137713-C-A

88624051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123137713-C-T

88624094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137766-C-T

88624095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137767-G-A

88624100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137772-G-A

88624100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137772-G-T

88624111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137783-G-A

88624111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137783-G-T

http://identifiers.org/hco/16/GRCh38#88624115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123137787-C-A

88624115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137787-C-T

88624132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137803-C-G

http://identifiers.org/hco/16/GRCh38#88624461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123137936-C-A

88624461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137936-C-T

http://identifiers.org/hco/16/GRCh38#88624520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123137961-C-A

88624520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137961-C-G

88624520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137961-C-T

88624573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123137992-T-C

88627370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139452-T-C

88627428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139525-G-A

88627428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139525-G-T

88627454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139551-T-A

88627454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139551-T-C

88627510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139602-T-C

http://identifiers.org/hco/16/GRCh38#88627517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123139609-A-C

88627517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139609-A-G

88627581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139685-C-T

88627600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123139704-T-G

88627939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123140021-C-T

88627958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123140040-C-T

88627969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123140051-T-C

88627976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123140058-A-G

88627984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123140066-A-G

88628008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123140090-A-G

88628035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123140117-G-A

88628038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123140120-A-G

88628052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123140134-C-G

88628052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123140134-C-T

88628540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123140400-G-T

88628761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123140599-G-A

88630534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123142824-G-C

88630536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123142826-G-A

88630979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123143147-G-T

88631219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123143333-C-T

88631257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123143371-T-G

88631339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 123143464-G-A

88631339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 123143464-G-T

88631503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123143647-A-G

http://identifiers.org/hco/16/GRCh38#88631577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123143729-C-A

88631577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123143729-C-T

http://identifiers.org/hco/16/GRCh38#88631673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123143790-C-A

88631673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 123143790-C-T

http://identifiers.org/hco/16/GRCh38#88631710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123143829-C-A

88631798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123143921-G-A

88631798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123143921-G-T

88631934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123144069-G-A

88631934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123144069-G-T