34105689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 103591505-A-G

http://identifiers.org/hco/11/GRCh38#34105723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103591476-C-A

34105723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 103591476-C-T

http://identifiers.org/hco/11/GRCh38#34105796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103591388-C-A

34105796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103591388-C-G

34105815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103591370-G-C

34105815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103591370-G-T

34105853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103591333-T-C

34105872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103591316-A-G

34106147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103591073-G-A

34106712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103590226-C-G

34106712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103590226-C-T

http://identifiers.org/hco/11/GRCh38#34108222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103588125-C-A

http://identifiers.org/hco/11/GRCh38#34108400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103587939-C-A

34108400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587939-C-T

34108430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587909-G-C

34108462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587878-A-G

34108724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587635-G-A

http://identifiers.org/hco/11/GRCh38#34108787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103587558-C-A

34108787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103587558-C-T

34109867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103586553-T-C

34110202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103586279-G-A

34110361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103586186-C-G

34110361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103586186-C-T

http://identifiers.org/hco/11/GRCh38#34110523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103586057-A-C

34110523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103586057-A-T

34110532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103586052-G-T

http://identifiers.org/hco/11/GRCh38#34110624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103585971-C-A

34110624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103585971-C-T

34110740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103585843-T-G

34110980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103585607-G-C

34111617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103585064-T-C

34111974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103584625-T-C

34112316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103584364-G-A

http://identifiers.org/hco/11/GRCh38#34112349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103584330-A-C

34112533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103584153-C-G

http://identifiers.org/hco/11/GRCh38#34112904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103583760-A-C

http://identifiers.org/hco/11/GRCh38#34112947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103583715-C-A

34113380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103583219-G-A

34113486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103583119-A-G

34113668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103583093-G-A

34113668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103583093-G-T

http://identifiers.org/hco/11/GRCh38#34113927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103582863-C-A

34113927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103582863-C-T

34113935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103582855-G-A

34113935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103582855-G-T

http://identifiers.org/hco/11/GRCh38#34113947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103582843-C-A

34114070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103582754-A-G

34114382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103582400-C-T

34114389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103582393-A-G

34114746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103582059-C-T

34115332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103581055-C-G

34115460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103580929-T-C

34115815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 103580634-T-C

34115949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103580497-T-G

http://identifiers.org/hco/11/GRCh38#34115996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103580332-C-A

34116004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103580324-A-G

34117884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578910-G-T

34118041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578744-G-A

34118041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578744-G-C

34118041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578744-G-T

34118157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578666-A-G

34118157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578666-A-T

34118317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578505-G-A

34118317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578505-G-T

34118329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578495-G-A

34118358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578462-G-A

34118472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: missense variant
orthologous variants: 103578353-T-A

34118472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: missense variant
orthologous variants: 103578353-T-G

http://identifiers.org/hco/11/GRCh38#34118555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103578256-C-A

34118555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578256-C-G

34118555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578256-C-T

34118607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103578167-G-A

34119016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103577528-A-G

34119087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103577480-C-T

34119126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103577453-T-G

34119138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103577441-G-C

34119856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103576629-C-T

34119910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103576595-G-A

34119951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103576552-T-C

34120205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103576371-G-T

34120398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103576195-G-A

34120792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103575678-A-T

34120996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103575528-C-T

34121160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103575394-C-G

34121238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103575325-A-T

34121273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103575285-T-C

34122250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103574958-A-G

http://identifiers.org/hco/11/GRCh38#34122289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103574926-A-C

34122289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103574926-A-G

34122406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103574812-G-A

http://identifiers.org/hco/11/GRCh38#34123661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103573815-C-A

34123671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573804-A-G

34123671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573804-A-T

34124426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573363-G-A

34124426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573363-G-T

34124427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573362-T-C

34124437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573349-G-A

34124437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573349-G-C

34124439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573347-G-C

34124456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573330-T-A

34124518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573268-A-T

34124520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573266-T-C

34124792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103573019-A-G

34125203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103572400-T-G

34127341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570352-T-C

34127341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570352-T-G

34127370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570322-A-G

34127403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570294-G-A

34127403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570294-G-T

http://identifiers.org/hco/11/GRCh38#34127410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103570287-C-A

34127410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570287-C-G

34127410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570287-C-T

34127424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570269-G-A

34127425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570268-T-A

34127665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103570030-T-G

http://identifiers.org/hco/11/GRCh38#34127725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103569979-C-A

34127725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103569979-C-G

34127725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103569979-C-T

34127835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103569881-C-G

34127835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103569881-C-T

34127850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103569872-T-C

34128066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103569686-T-A

34129051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103568001-G-A

http://identifiers.org/hco/11/GRCh38#34129093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103567959-C-A

34129093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103567959-C-G

34129473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103567574-G-T

34129609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103567480-T-A

34129613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103567476-T-C

http://identifiers.org/hco/11/GRCh38#34129636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103567453-C-A

34129636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103567453-C-G

34130090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103567101-T-G

34130669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103565397-T-C

34130688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103565376-A-G

34130688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103565376-A-T

34130814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 103565332-T-C

34131072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103565130-G-T

34131146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103565075-G-C

34131235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103565006-A-G

34131235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103565006-A-T

34131330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564914-T-C

34131330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564914-T-G

34131383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 103564866-C-G

34131383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 103564866-C-T

34131398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant
orthologous variants: 103564851-G-A

34131398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant
orthologous variants: 103564851-G-T

34131434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant
orthologous variants: 103564815-G-A

34131434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant
orthologous variants: 103564815-G-T

34131452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant
orthologous variants: 103564797-C-G

34131457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103564792-T-C

34131495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant
orthologous variants: 103564754-T-C

34131560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564694-G-T

http://identifiers.org/hco/11/GRCh38#34131690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103564544-C-A

34131690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564544-C-G

34131690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564544-C-T

34131719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564515-C-T

34131829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564415-G-A

34132070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564239-G-A

34132070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564239-G-C

34132070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564239-G-T

34132085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564224-G-A

34132085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103564224-G-T

34132117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 103564190-A-G

34132350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103563966-T-G

http://identifiers.org/hco/11/GRCh38#34132774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103563625-A-C

34132774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103563625-A-G

34132782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103563617-C-T

http://identifiers.org/hco/11/GRCh38#34132877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103563520-A-C

34132877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103563520-A-T

34132927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103563471-A-G

34132933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103563465-A-G

34133272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103563157-G-T

34133777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562795-T-C

34134246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562673-C-T

34134310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562605-C-T

34134391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant
orthologous variants: 103562526-G-T

34134457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562457-G-A

34134457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562457-G-C

34134457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562457-G-T

http://identifiers.org/hco/11/GRCh38#34134467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103562431-A-C

34134467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562431-A-G

34134591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562311-T-C

http://identifiers.org/hco/11/GRCh38#34134655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103562232-C-A

34134665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562222-A-T

34134688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562198-G-A

34134688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562198-G-T

34134722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562171-G-C

34134722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562171-G-T

34134726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562167-G-C

34134726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562167-G-T

34134737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562155-G-A

34134737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562155-G-T

34134740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103562152-T-G

34134962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103561952-A-G

34134998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103561923-A-G

34135129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103561804-A-T

34135346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103561598-T-C

34135346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103561598-T-G

34136401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103561194-C-G

34136401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103561194-C-T

34136764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103560864-C-G

34136857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103560775-A-G

34136862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103560770-G-T

http://identifiers.org/hco/11/GRCh38#34136871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103560761-C-A

34136960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103560660-G-C

34136968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103560652-A-G

http://identifiers.org/hco/11/GRCh38#34137115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103560509-C-A

34137115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103560509-C-T

34137137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103560490-T-A

34137261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103560377-G-A

34137918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103559511-C-T

34137955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103559491-G-T

34138143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103559324-G-A

34138467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103559052-G-A

34138659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103558863-G-A

http://identifiers.org/hco/11/GRCh38#34138955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103558560-C-A

http://identifiers.org/hco/11/GRCh38#34138973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103558539-A-C

34138973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103558539-A-G

34138973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103558539-A-T

34139163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103558467-G-A

34139163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103558467-G-C

34139163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103558467-G-T

34139237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103558393-C-T

34139389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103558252-C-T

34139618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103558100-G-A

34139618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103558100-G-T

34140330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103557300-T-A

34140330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103557300-T-C

34140338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103557292-G-A

34140338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103557292-G-C

34140338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103557292-G-T

http://identifiers.org/hco/11/GRCh38#34140349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103557281-C-A

34140349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103557281-C-G

34140349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103557281-C-T

34140711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556930-A-G

34140711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556930-A-T

34140851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556812-T-C

34140892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556762-T-G

34140942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556713-G-A

34140942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556713-G-T

34140961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556699-A-G

34140975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556686-T-A

http://identifiers.org/hco/11/GRCh38#34140991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103556673-C-A

http://identifiers.org/hco/11/GRCh38#34141510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103556289-C-A

34141699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556125-C-G

34141699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103556125-C-T

34141764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant
orthologous variants: 103556060-G-A

34141849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103555982-A-G

34141875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103555955-G-A

34141875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron variant
orthologous variants: 103555955-G-C

34142006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103555726-G-A

34142006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103555726-G-T

34142056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103555687-G-A

34142056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103555687-G-T

http://identifiers.org/hco/11/GRCh38#34142245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103555534-C-A

34142245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103555534-C-T

34143126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554869-T-C

34143229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554791-C-T

http://identifiers.org/hco/11/GRCh38#34143284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103554750-C-A

34143506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103554557-G-A

34143541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554526-G-T

http://identifiers.org/hco/11/GRCh38#34143552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103554510-C-A

34143676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554420-T-A

34143676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554420-T-G

34144568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553832-C-T

http://identifiers.org/hco/11/GRCh38#34144965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103553501-C-A

34145136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553355-C-G

34145136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553355-C-T

34145270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553022-A-G

34145676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552604-C-T

34145962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552379-G-A

34145982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552366-G-A

http://identifiers.org/hco/11/GRCh38#34146245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103552127-C-A

34146245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103552127-C-G

34146247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103552125-G-T

http://identifiers.org/hco/11/GRCh38#34146391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103551991-C-A

34146401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551983-G-A

34146443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551948-T-C

34146548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551885-T-C

34146548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551885-T-G

http://identifiers.org/hco/11/GRCh38#34146581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103551854-C-A

34146581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551854-C-G

34146581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551854-C-T

http://identifiers.org/hco/11/GRCh38#34146658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103551790-C-A

34146658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551790-C-T

34146659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551789-G-A

34146659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551789-G-T

34146668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3 prime UTR variant
orthologous variants: 103551780-G-A

34146774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103551733-A-G

http://identifiers.org/hco/11/GRCh38#34146799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103551708-C-A

34146799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103551708-C-T

34146846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103551658-T-C

34146861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103551643-A-G

34146924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29830
most severe consequence: non coding transcript exon variant
orthologous variants: 103551586-T-C