24819485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4263206-A-T

http://identifiers.org/hco/2/GRCh38#24819619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4263118-C-A

24819619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4263118-C-T

http://identifiers.org/hco/2/GRCh38#24819623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4263114-C-A

24819623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4263114-C-G

24819664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4263072-G-A

24819664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4263072-G-T

24819715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4263023-T-C

http://identifiers.org/hco/2/GRCh38#24819745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4262993-A-C

24819745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4262993-A-G

24819745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4262993-A-T

24819749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4262989-G-A

24819749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4262989-G-C

24819749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4262989-G-T

24819843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4262899-G-A

24819843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4262899-G-T

http://identifiers.org/hco/2/GRCh38#24819901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4262817-C-A

http://identifiers.org/hco/2/GRCh38#24820077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4262640-C-A

24820077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4262640-C-T

24820116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 4262601-T-G

24820127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4262590-G-A

24820127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4262590-G-C

24820127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4262590-G-T

http://identifiers.org/hco/2/GRCh38#24820149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4262571-C-A

24820149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4262571-C-G

24820149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4262571-C-T

24820153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4262567-G-A

24820153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4262567-G-T

http://identifiers.org/hco/2/GRCh38#24820600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4262329-C-A

24820600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4262329-C-T

http://identifiers.org/hco/2/GRCh38#24821120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4261867-C-A

24821148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261837-C-G

http://identifiers.org/hco/2/GRCh38#24821406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4261673-C-A

http://identifiers.org/hco/2/GRCh38#24821968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4261232-A-C

24822076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261144-T-A

24822076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261144-T-C

24822076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261144-T-G

http://identifiers.org/hco/2/GRCh38#24822084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4261136-C-A

24822084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261136-C-T

24822129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261099-A-G

24822156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261070-A-G

24822161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261064-A-G

http://identifiers.org/hco/2/GRCh38#24822179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4261047-C-A

24822179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4261047-C-G

24822179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4261047-C-T

24822251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4261007-G-T

http://identifiers.org/hco/2/GRCh38#24822341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4260971-C-A

24822341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4260971-C-T

24822480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260914-C-T

24822704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4260713-C-G

24822704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4260713-C-T

http://identifiers.org/hco/2/GRCh38#24822720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4260696-C-A

24822720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260696-C-T

http://identifiers.org/hco/2/GRCh38#24822728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4260688-C-A

24822728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260688-C-T

http://identifiers.org/hco/2/GRCh38#24822738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4260678-C-A

24822738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260678-C-T

http://identifiers.org/hco/2/GRCh38#24822775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4260651-C-A

24822775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260651-C-T

24822852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260592-G-A

http://identifiers.org/hco/2/GRCh38#24823094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4260417-A-C

24823094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260417-A-G

24823261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4260286-C-T

24824026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259737-C-G

24824195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259604-C-T

24824295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259513-T-C

24824333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259483-G-A

24824333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259483-G-C

24824343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259473-G-A

24824457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4259382-C-T

24824582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259261-G-A

24824582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259261-G-T

24825150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259061-A-G

24825196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259020-G-A

24825695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258878-T-C

24825734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258834-G-A

24825734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258834-G-T

24825835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258808-G-A

24825835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258808-G-T

24825949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258738-T-C

24826137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4258567-G-A

http://identifiers.org/hco/2/GRCh38#24826213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4258516-C-A

http://identifiers.org/hco/2/GRCh38#24826217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4258512-C-A

24826217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258512-C-T

http://identifiers.org/hco/2/GRCh38#24826240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4258466-C-A

24826240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258466-C-T

24826250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258452-A-G

http://identifiers.org/hco/2/GRCh38#24826253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4258449-C-A

24826253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258449-C-T

24826256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258446-T-C

http://identifiers.org/hco/2/GRCh38#24826277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4258437-C-A

24826277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258437-C-T

24826286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258428-T-A

24826286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258428-T-C

24826286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258428-T-G

http://identifiers.org/hco/2/GRCh38#24826319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4258400-A-C

24826319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258400-A-G

http://identifiers.org/hco/2/GRCh38#24826695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4258094-C-A

24826695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258094-C-G

24826705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258084-T-A

24826705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258084-T-C

24826705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258084-T-G

http://identifiers.org/hco/2/GRCh38#24826706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4258083-C-A

24826706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258083-C-G

24826706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4258083-C-T

24826718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4258071-G-A

24826718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4258071-G-C

24826732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4258057-T-C

24826740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4258049-G-A

24826740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4258049-G-T

24826752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4258037-T-C

24827196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4257352-A-G

24827214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4257336-C-T

24827311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4257260-G-A

24827347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4257224-C-T

24827379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4257168-C-T

http://identifiers.org/hco/2/GRCh38#24827414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4257117-C-A

24827496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4257023-T-A

24827496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4257023-T-C

http://identifiers.org/hco/2/GRCh38#24827521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4257001-C-A

24827521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4257001-C-T

24827572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4256947-G-A

24827572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4256947-G-T

24827574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4256945-A-G

24827636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4256883-G-A

24827636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4256883-G-T

24827714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4256809-G-A

24827714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4256809-G-C

24827714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4256809-G-T

24827793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4256734-A-T

http://identifiers.org/hco/2/GRCh38#24828115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4256409-C-A

24828115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4256409-C-G

24828115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4256409-C-T

http://identifiers.org/hco/2/GRCh38#24828262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4256281-C-A

24828262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4256281-C-T

24828263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4256280-G-A

24830201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4255250-T-A

24830201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4255250-T-C

24830213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4255237-G-A

http://identifiers.org/hco/2/GRCh38#24830249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4255211-C-A

24830249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4255211-C-T

24830280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4255191-C-G

24830572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4254951-G-T

24830606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4254923-G-T

http://identifiers.org/hco/2/GRCh38#24830806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4254739-A-C

24830806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4254739-A-G

24831526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253724-G-A

24831526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253724-G-T

http://identifiers.org/hco/2/GRCh38#24831535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4253715-C-A

24831549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253701-G-T

24831645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253616-A-G

24831647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253614-A-G

24831652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253609-T-C

24831698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4253563-G-A

24831778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253483-G-C

24831778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253483-G-T

24832239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4253350-T-C

http://identifiers.org/hco/2/GRCh38#24832323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4253266-C-A

24832378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253207-G-A

24832400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253201-G-A

24832407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253194-G-A

24832407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4253194-G-T

24832815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4252771-A-G

http://identifiers.org/hco/2/GRCh38#24833072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4252551-C-A

24833155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4252458-C-T

24833254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4252386-G-A

24833292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4252353-C-T

24833313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4252332-A-T

24833587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4252105-T-C

http://identifiers.org/hco/2/GRCh38#24833875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4251866-A-C

24834092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4251653-A-G

24834124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4251627-G-C

http://identifiers.org/hco/2/GRCh38#24834421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4251384-C-A

24834421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4251384-C-G

24834421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4251384-C-T

24834593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4251233-A-G

http://identifiers.org/hco/2/GRCh38#24834608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4251218-A-C

24834711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4251116-G-A

24834711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4251116-G-T

24834721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4251106-T-C

24834824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4251012-T-C

24834824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4251012-T-G

http://identifiers.org/hco/2/GRCh38#24835042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4250803-C-A

24835042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4250803-C-T

24835270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4250680-G-A

24835272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4250678-A-G

24836198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249984-C-G

http://identifiers.org/hco/2/GRCh38#24836199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4249983-C-A

24836301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249904-G-A

24836939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4249409-T-G

24836954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4249394-C-G

http://identifiers.org/hco/2/GRCh38#24838395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4248494-A-C

24838395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4248494-A-T

24838426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4248486-G-A

24838515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4248400-T-G

24838628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4248287-T-C

24838708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4248210-C-T

24838721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4248197-G-A

24838721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4248197-G-T

http://identifiers.org/hco/2/GRCh38#24838722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4248196-C-A

24838789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4248131-G-A

24839815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246981-A-G

24839824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246972-A-T

24839933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4246860-T-C

http://identifiers.org/hco/2/GRCh38#24839960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4246833-C-A

24839960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4246833-C-T

http://identifiers.org/hco/2/GRCh38#24840075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4246718-C-A

24840075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246718-C-G

24840075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246718-C-T

24840164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246630-G-T

24840347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246487-A-G

http://identifiers.org/hco/2/GRCh38#24840657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4245760-C-A

24840657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245760-C-T

http://identifiers.org/hco/2/GRCh38#24840697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4245725-C-A

24840697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245725-C-G

24840697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245725-C-T

24840724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245697-G-A

24840724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245697-G-C

http://identifiers.org/hco/2/GRCh38#24840727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4245694-C-A

24840727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245694-C-T

24840728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245693-A-G

24840854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245584-C-T

24840973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245505-A-G

24841019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245475-A-T

24841067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245450-G-C

24841104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245394-C-T

24841111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245387-A-G

24841111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245387-A-T

http://identifiers.org/hco/2/GRCh38#24841160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4245345-A-C

24841160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245345-A-T

http://identifiers.org/hco/2/GRCh38#24841161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4245344-C-A

http://identifiers.org/hco/2/GRCh38#24841188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4245326-C-A

24841188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245326-C-G

24841188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245326-C-T

24841208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245309-G-A

24841210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245307-G-A

24841210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245307-G-T

24841399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245117-G-A

24841544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244986-C-G

24841544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244986-C-T

24841578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4244953-G-T

24841706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244824-A-G

24841706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244824-A-T

24841707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244823-G-A

http://identifiers.org/hco/2/GRCh38#24841782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4244786-C-A

24841782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244786-C-T

24841800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244771-A-G

http://identifiers.org/hco/2/GRCh38#24841944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4244682-C-A

http://identifiers.org/hco/2/GRCh38#24842103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4244549-C-A

24842103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244549-C-T

24842109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244543-C-T

24842129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244511-G-A

24842129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244511-G-T

24842146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244493-T-A

24842166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244473-G-A

24842174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244467-C-T

24842176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244465-G-A

24842176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244465-G-T

24842387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4244312-G-A

http://identifiers.org/hco/2/GRCh38#24842569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4244141-C-A

24842569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4244141-C-T

http://identifiers.org/hco/2/GRCh38#24842619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4244092-C-A

24842619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244092-C-G

24842619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244092-C-T

24842739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244000-G-A

24842825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243939-G-T

24843108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243646-C-T

24843643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243392-G-A

24843726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243299-G-A

24847555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242666-C-G

24847777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242553-G-C

24847923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242421-G-A

24847935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242415-C-T

24849335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241588-C-T

24849341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241582-C-T

24849472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241463-G-C

24854355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239663-G-A

24854458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239577-C-G

24854648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239399-G-A

24854648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239399-G-C

24855125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239176-G-A

24855162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239155-T-C

24855356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239010-T-C

24855526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4238840-C-T

24855618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4238761-C-T

24856049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4238318-A-G

24856081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4238286-G-A

24856173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4238190-T-A

24856173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4238190-T-G

24856472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4234952-A-G

24856523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4234902-G-A

24856523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4234902-G-T

24857264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4234607-C-T

24859014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4230500-C-G

24859049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4230458-G-A

24859240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4230074-G-A

24859549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4229806-A-T

24859550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4229805-A-T

24860001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4229429-G-A

24860084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4229360-T-A

24860092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4229352-T-C

24860257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4229198-A-G

24860310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4229146-T-C

24860424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4229035-G-A

24860504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228974-G-A

24860593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228892-C-T

24860594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228891-T-C

24861585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228356-G-A

24861585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228356-G-C

http://identifiers.org/hco/2/GRCh38#24861727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4228269-C-A

24861727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228269-C-T

24861754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228244-G-C

24861769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228232-G-A

24861854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4228154-G-T

24862026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227983-C-T

24862036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227973-A-G

24862059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227950-G-A

24862114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227896-C-T

24862142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227872-G-C

24862196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227825-C-T

24863914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227768-G-T

24864340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227617-A-T

24864564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227408-C-T

http://identifiers.org/hco/2/GRCh38#24864588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4227381-A-C

24864800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4227204-T-C

24872592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4223580-A-G

24872610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4223562-A-G

http://identifiers.org/hco/2/GRCh38#24872649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4223523-C-A

24872649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4223523-C-T

24872734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4223438-A-T

24872757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4223419-G-A

http://identifiers.org/hco/2/GRCh38#24872895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4223285-C-A

24873420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4222359-C-T

24873464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4222319-G-A

http://identifiers.org/hco/2/GRCh38#24873602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4222176-C-A

24874034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4221490-G-A

24874051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4221474-G-C

24874095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4221428-G-A

24874209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4221281-T-C

24875216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4219967-C-T

24875274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4219931-G-A

24875274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4219931-G-C

24875609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4219630-G-A

24875824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4219484-T-C

24875913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4218461-C-T

24876362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4217757-C-T

http://identifiers.org/hco/2/GRCh38#24876734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4217410-C-A

24876976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4217186-C-T

24877038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4217143-C-T

24877240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4216977-G-A

24877280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4216938-C-G

24877413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4216844-C-T

24878632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4215127-T-C

http://identifiers.org/hco/2/GRCh38#24878760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4214996-C-A

24878845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4214905-C-T

24878910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4214827-G-A

24878950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4214768-A-G

24879442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213907-G-A

24879442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213907-G-T

24879490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213840-C-G

24879529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213801-C-G

24879591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213732-G-A

24879812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213501-G-A

24879918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213432-A-G

http://identifiers.org/hco/2/GRCh38#24879925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4213425-C-A

24880268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213127-G-C

24880299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4213102-G-T

24880421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4212980-T-A

24882698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4211971-G-A

24882717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4211952-G-A

24883878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4210685-A-G

http://identifiers.org/hco/2/GRCh38#24883882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4210681-C-A

24883957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4210606-G-A

24884332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4209937-T-C

24885832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4209423-G-C

24905112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4198061-G-A

http://identifiers.org/hco/2/GRCh38#24905560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4196553-C-A

24907250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4195614-G-A

24907400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4195482-C-G

24907484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4195414-G-C

24907527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4195389-C-T

24908510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4195089-T-C

http://identifiers.org/hco/2/GRCh38#24908612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4194869-A-C

24908624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4194857-A-G

24908886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4194710-C-T

http://identifiers.org/hco/2/GRCh38#24908904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4194698-C-A

24908904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4194698-C-T

http://identifiers.org/hco/2/GRCh38#24908912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4194690-C-A

24908961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4194659-C-G

http://identifiers.org/hco/2/GRCh38#24909812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4191521-C-A

24909838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4191495-T-C

24909987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4191344-T-C

24912619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4190637-G-A

24912624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4190632-T-C

24912741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4190502-G-A

24912883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4190161-C-G

24912883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4190161-C-T

24912888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4190156-G-A

24912943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4190091-A-G

24912968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4190061-A-G

24913072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4189995-T-C

24913197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4189873-C-T

24913514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4189605-T-C

24913897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4189424-T-C

24915047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4188833-T-C

http://identifiers.org/hco/2/GRCh38#24917572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4185683-A-C

24917951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4185333-G-A

24918684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4184627-T-C

http://identifiers.org/hco/2/GRCh38#24918833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4184478-A-C

24918881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4184430-T-C

24918881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4184430-T-G

24918947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4184364-G-T

24918991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4184320-G-A

24918991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4184320-G-C

24918991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4184320-G-T

24918996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4184315-G-T

24919035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4184295-A-T

24919049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4184281-A-G

http://identifiers.org/hco/2/GRCh38#24919358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4184017-C-A

http://identifiers.org/hco/2/GRCh38#24919377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4183998-C-A

24919377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4183998-C-T

24919475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4183921-T-C

24919475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4183921-T-G

http://identifiers.org/hco/2/GRCh38#24919481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4183915-C-A

24919481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4183915-C-T

http://identifiers.org/hco/2/GRCh38#24919651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4183760-C-A

24919651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4183760-C-G

24919651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4183760-C-T

http://identifiers.org/hco/2/GRCh38#24919723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4183678-C-A

24919723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4183678-C-T

24919734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4183668-G-A

24919767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4183635-T-C

24919883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 234
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4183522-G-T