http://identifiers.org/hco/3/GRCh38#195720895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#32617899-C-A

195720895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32617899-C-G

195720895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32617899-C-T

http://identifiers.org/hco/3/GRCh38#195720917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#32617857-A-C

195720917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32617857-A-G

http://identifiers.org/hco/3/GRCh38#195720944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#32617830-A-C

195720944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32617830-A-T

195720967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32617807-A-G

195720980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32617794-T-C

195720983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32617791-T-C

195720983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32617791-T-G

195720995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32617779-G-A

195720995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32617779-G-T

195721062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32617706-G-A

195721062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32617706-G-T

195721063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32617705-G-A

195721063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32617705-G-C

195721063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32617705-G-T

http://identifiers.org/hco/3/GRCh38#195721119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32617653-C-A

195721119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617653-C-T

195721255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617571-C-T

195721326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617524-C-T

195721435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32617445-G-A

195721570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617342-T-C

195721570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617342-T-G

195721587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617325-G-C

http://identifiers.org/hco/3/GRCh38#195721634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32617278-A-C

195721638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617274-T-C

195721660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617252-G-A

195721660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617252-G-T

195721669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617243-T-C

195724337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615592-G-A

195724337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615592-G-T

http://identifiers.org/hco/3/GRCh38#195724361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32615562-C-A

195724361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615562-C-T

195724376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615547-T-C

http://identifiers.org/hco/3/GRCh38#195724408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32615528-C-A

195724408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615528-C-T

195724438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615504-G-A

195724438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615504-G-C

http://identifiers.org/hco/3/GRCh38#195724481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32615460-C-A

195724481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615460-C-T

195724518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615424-T-G

http://identifiers.org/hco/3/GRCh38#195724604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32615360-C-A

195724604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615360-C-T

195724613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615351-T-A

195724613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32615351-T-G

195724772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32615163-A-G

195724772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32615163-A-T

http://identifiers.org/hco/3/GRCh38#195724854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32615081-A-C

195724854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32615081-A-G

195724891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32614609-A-G

195724892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614608-A-G

http://identifiers.org/hco/3/GRCh38#195724941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#32614559-C-A

195724941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614559-C-T

195724970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614533-G-A

195724975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614528-G-T

http://identifiers.org/hco/3/GRCh38#195725004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32614499-A-C

195725004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614499-A-G

http://identifiers.org/hco/3/GRCh38#195725016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32614487-C-A

http://identifiers.org/hco/3/GRCh38#195725112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32614391-A-C

195725112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: 32614391-A-G

195725112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: 32614391-A-T

195725162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: 32614341-A-G

195725872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: synonymous variant
orthologous variants: 32614255-T-C

195725925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: 32614205-A-T

195725926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: 32614204-C-G

195725926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: synonymous variant
orthologous variants: 32614204-C-T

195725950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: synonymous variant
orthologous variants: 32614180-G-A

195726018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: 32614112-C-G

195726018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: 32614112-C-T

195726053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense variant
orthologous variants: 32614077-G-A

http://identifiers.org/hco/3/GRCh38#195726188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32613951-C-A

195726188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32613951-C-G

195726188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32613951-C-T

195726288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32613851-A-G

195726344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32613789-C-G

195726344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32613789-C-T

195726410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32613723-A-G

195726435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32613698-C-T

195726529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32613604-G-A

195726529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32613604-G-T

http://identifiers.org/hco/3/GRCh38#195726531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32613602-C-A

195726531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32613602-C-T

195726655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613501-G-A

195726655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613501-G-T

195726659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613497-A-G

195726659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613497-A-T

195726660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613496-G-A

195726660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613496-G-C

195726660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613496-G-T

http://identifiers.org/hco/3/GRCh38#195726681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32613474-C-A

195726681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613474-C-G

195726681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613474-C-T

195726761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613394-G-A

195726962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612975-C-G

195726962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612975-C-T

195727008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612931-A-G

195727016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612923-G-A

195729607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32610595-C-T

195729622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32610581-T-C

195729707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32610500-G-A

195729707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32610500-G-T

195729769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610449-T-C

195729769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610449-T-G

http://identifiers.org/hco/3/GRCh38#195729799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32610425-C-A

195729799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610425-C-T

http://identifiers.org/hco/3/GRCh38#195729817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32610407-C-A

195729817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610407-C-T

195729844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610382-A-G

195729844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610382-A-T

195729884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610363-G-T

http://identifiers.org/hco/3/GRCh38#195729908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32610340-C-A

195729908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610340-C-T

195729957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610292-G-A

195729957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610292-G-C

195729957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610292-G-T

195729958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610291-T-A

195729958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610291-T-C

195729958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610291-T-G

195729962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610286-T-A

195729962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610286-T-C

195729962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610286-T-G

195730022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610232-A-G

195730022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610232-A-T

195730052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610202-G-A

195730052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610202-G-T

http://identifiers.org/hco/3/GRCh38#195730080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32610175-C-A

195730095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610160-T-A

195730095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610160-T-C

195730095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32610160-T-G

195730147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32610125-T-A

195730147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32610125-T-G

195730167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32610103-G-A

195730167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32610103-G-C

195730167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32610103-G-T

http://identifiers.org/hco/3/GRCh38#195730188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32610082-C-A

195730188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32610082-C-T

195730830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32608748-G-A

195730843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32608732-T-C

195730925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32608667-G-A

http://identifiers.org/hco/3/GRCh38#195730968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32608623-C-A

195731216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32608494-C-T

195731263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32608457-T-C

195731297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32608423-G-T

195731307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32608413-G-C

195731311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32608410-T-C

195731655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32607692-A-G

195731674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32607673-T-A

195731964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32607413-G-T

195732761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/3/GRCh38#195732924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32606918-C-A

195732924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606918-C-T

195732949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606893-A-G

http://identifiers.org/hco/3/GRCh38#195733044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32606855-C-A

195733044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606855-C-T

195733089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606821-G-C

http://identifiers.org/hco/3/GRCh38#195733093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32606817-C-A

195733093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606817-C-G

195733093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606817-C-T

195733119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606792-T-C

195733128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606783-A-G

http://identifiers.org/hco/3/GRCh38#195733130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32606781-C-A

195733130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606781-C-G

http://identifiers.org/hco/3/GRCh38#195733155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32606756-C-A

195733155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32606756-C-T

http://identifiers.org/hco/3/GRCh38#195733170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#32606741-C-A

195733195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, missense_variant
orthologous variants: 32606716-T-A

195733195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32606716-T-C

195733269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606641-C-T

http://identifiers.org/hco/3/GRCh38#195733271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32606638-C-A

195733275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606634-G-T

195733279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606630-G-A

195733279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606630-G-C

195733279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606630-G-T

195733281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606628-G-A

195733281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606628-G-T

195733304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606605-G-T

195733331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606581-A-G

195733331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606581-A-T

195733471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606442-G-A

195733471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606442-G-T

http://identifiers.org/hco/3/GRCh38#195733506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32606407-A-C

195733542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606371-G-C

195733542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606371-G-T

195733552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32606360-G-T

195733620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606288-T-A

195733620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606288-T-C

195733620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606288-T-G

195733644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606283-G-C

195733644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: intron variant
orthologous variants: 32606283-G-T

195735117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32605248-T-A

195735117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32605248-T-G

195735266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32605105-C-T

195735274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32605097-T-G

195735368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32605002-G-C

195735477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604895-G-A

195735506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604865-C-T

195735564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604801-G-A

195735565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604800-C-T

195735684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604671-A-G

195735717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604582-C-T

http://identifiers.org/hco/3/GRCh38#195735794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32604445-C-A

195735794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604445-C-T

http://identifiers.org/hco/3/GRCh38#195735814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32604425-C-A

195735814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604425-C-T

195735847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604386-T-C

195735858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604375-A-G

195735950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604197-A-T

195735965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604181-G-C

195736017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32604129-C-T

195736063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32603998-C-G

195736072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32603989-G-A

195736072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32603989-G-C

195736077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32603984-G-A

195736081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23282
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32603980-T-G