54901798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70105216-T-C

54901798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70105216-T-G

54901880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70105138-C-T

http://identifiers.org/hco/18/GRCh38#54902338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70104785-C-A

54902383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104744-G-A

54902513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104618-A-G

54902580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104551-C-T

54902607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104522-G-A

54902672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104458-T-A

54902684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104442-C-T

54902707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104419-A-G

54902731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104394-T-C

54902733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104392-G-C

54902740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104385-T-G

54902770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104352-A-G

54902864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104259-A-G

54902964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70104161-A-G

54903039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70103838-T-C

54903075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3 prime UTR variant
orthologous variants: 70103815-C-T

54903514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102891-A-G

http://identifiers.org/hco/18/GRCh38#54903556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70102850-C-A

54903595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102814-A-G

54903609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102800-C-G

54903613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102796-A-G

54903621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102789-G-C

54903621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102789-G-T

http://identifiers.org/hco/18/GRCh38#54903916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70102505-C-A

54904029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102440-A-T

http://identifiers.org/hco/18/GRCh38#54904070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70102401-A-C

54904140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102333-T-C

54904264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70102200-G-T

54904418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 70102044-G-A

54904418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 70102044-G-T

54904431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70102031-C-T

54904444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70102014-A-G

54904458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70102000-A-T

54904541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70101906-G-A

54904543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70101904-G-C

54904543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70101904-G-T

54904553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70101892-T-A

54904553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70101892-T-C

http://identifiers.org/hco/18/GRCh38#54904659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70101792-A-C

54906405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70101233-C-T

54906461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70101177-C-T

54906567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70101056-A-G

54907102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70100614-T-A

54907102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70100614-T-C

54907148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70100568-G-C

54907694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70100026-G-A

54907694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70100026-G-T

54907708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70100011-T-C

54907725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099988-G-A

54907725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099988-G-T

http://identifiers.org/hco/18/GRCh38#54907777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70099944-A-C

54907777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099944-A-G

54907777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099944-A-T

54907821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 70099900-A-G

54907893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099825-T-C

54907894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099824-A-G

54907925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099793-G-A

54907925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099793-G-T

http://identifiers.org/hco/18/GRCh38#54907934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70099776-C-A

54907947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099763-G-A

54907947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099763-G-T

http://identifiers.org/hco/18/GRCh38#54907949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70099761-C-A

54907949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099761-C-T

54907962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099748-A-G

54908192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099574-G-T

54908212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099554-C-T

54908260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099506-T-C

54908359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099433-G-A

54908375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70099418-G-A

54911524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70097952-A-T

54911675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70097800-T-C

54911703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70097772-G-A

54911989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70097506-A-G

54912319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70097184-C-T

http://identifiers.org/hco/18/GRCh38#54912461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70097048-C-A

54917273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70095137-A-G

54917424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70095022-A-G

54917686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094800-T-C

http://identifiers.org/hco/18/GRCh38#54917838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70094687-C-A

54917838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094687-C-T

54917844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094681-C-G

54917849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094676-A-T

54917893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094632-A-G

54917926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense variant
orthologous variants: 70094599-A-G

54917926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense variant
orthologous variants: 70094599-A-T

54917992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense variant
orthologous variants: 70094533-T-C

54918019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094506-G-A

54918019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094506-G-C

54918019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094506-G-T

http://identifiers.org/hco/18/GRCh38#54918025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70094500-A-C

54918025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094500-A-G

54918051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094472-A-G

54918129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094407-T-C

54918130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094406-T-A

54918130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70094406-T-G

54918937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093889-A-T

54919114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093718-G-A

http://identifiers.org/hco/18/GRCh38#54919144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70093696-A-C

http://identifiers.org/hco/18/GRCh38#54919150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70093690-A-C

54919150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093690-A-G

http://identifiers.org/hco/18/GRCh38#54919161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70093680-C-A

54919246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093599-G-C

54919246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093599-G-T

http://identifiers.org/hco/18/GRCh38#54919465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70093411-C-A

54919465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093411-C-T

http://identifiers.org/hco/18/GRCh38#54919471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70093405-C-A

54919471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093405-C-T

54919481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093395-T-A

54919481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093395-T-G

54919487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093389-G-A

54919487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70093389-G-T

http://identifiers.org/hco/18/GRCh38#54919514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70093363-C-A

54922025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70092989-T-G

54926706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 70092075-G-A

http://identifiers.org/hco/18/GRCh38#54926707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70092074-A-C

54926744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70092036-G-A

54926776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70092007-A-G

54926777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70092006-T-A

54926781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70092002-A-G

54926971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70091860-T-C

http://identifiers.org/hco/18/GRCh38#54927181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70091086-C-A

54927757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70090285-A-G

54927941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70090111-A-G

54928005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70090029-G-A

54928022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70090012-G-A

54928081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089970-T-C

54928108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089943-G-A

54928108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089943-G-T

54928197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089851-T-C

54928237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089812-T-C

http://identifiers.org/hco/18/GRCh38#54928247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70089807-C-A

54928273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089782-G-T

54928376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089675-G-A

54928475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089586-G-A

54928562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089507-C-T

54928590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089456-G-A

54928590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70089456-G-T

54928811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: synonymous variant
orthologous variants: 70089122-T-C

54928811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: synonymous variant
orthologous variants: 70089122-T-G

54928812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense variant
orthologous variants: 70089121-G-A

54928812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense variant
orthologous variants: 70089121-G-T

54928899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70089031-T-C

54928924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70089014-T-A

54928984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088942-T-C

54928984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088942-T-G

54929031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088904-A-G

54929053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088882-T-C

54929228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088560-T-C

54929320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088454-A-G

54929430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088364-A-G

54929691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088177-G-A

54929741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088138-G-A

54929814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088071-T-G

54931191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70084632-G-A

54931224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70084598-G-C

54931303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70084528-A-G

http://identifiers.org/hco/18/GRCh38#54931336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70084506-A-C

54931347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70084495-G-A

54931602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70084054-G-A

54931955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70083698-G-A

54932023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70083584-A-G

54932051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70083557-G-A

54932119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70083488-A-G

54932912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081961-C-T

54932978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081871-T-C

http://identifiers.org/hco/18/GRCh38#54933379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70081772-C-A

54933379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081772-C-G

54933428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081709-C-T

54933597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081547-G-A

54933748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081415-C-T

54933761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081402-T-C

54933766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081397-C-T

54933894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70081267-A-G

http://identifiers.org/hco/18/GRCh38#54933989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70081114-A-C

54934098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080826-C-G

54934199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080742-T-C

54934250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080697-C-T

54934488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080491-G-A

54934698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080326-A-G

54934706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080318-T-A

http://identifiers.org/hco/18/GRCh38#54934739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70080304-C-A

54934739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080304-C-T

http://identifiers.org/hco/18/GRCh38#54934777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70080288-A-C

54934777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080288-A-G

54934777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080288-A-T

54934780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080285-G-A

54934780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080285-G-T

http://identifiers.org/hco/18/GRCh38#54934781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70080284-C-A

54934781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080284-C-T

54934801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080264-T-C

http://identifiers.org/hco/18/GRCh38#54934806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70080259-C-A

54934806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080259-C-T

54934818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 70080250-A-G

54934861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70080207-G-T

54934863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70080205-C-T

54935276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080064-A-T

54935283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70080057-A-T

54935384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70079952-T-C

54935428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70079912-T-C

http://identifiers.org/hco/18/GRCh38#54935593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079742-C-A

54936850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70079601-T-C

54936978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079468-G-T

54937009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079427-A-G

http://identifiers.org/hco/18/GRCh38#54937010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079426-A-C

54937049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079391-G-A

54937049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079391-G-C

54937049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079391-G-T

http://identifiers.org/hco/18/GRCh38#54937061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079381-C-A

54937061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079381-C-T

54937075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079367-T-C

54937086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079355-T-C

54937160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079286-A-G

http://identifiers.org/hco/18/GRCh38#54937161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079285-C-A

54937161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079285-C-T

http://identifiers.org/hco/18/GRCh38#54937182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079264-A-C

54937200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079246-T-G

http://identifiers.org/hco/18/GRCh38#54937208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079238-A-C

54937208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079238-A-G

54937208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079238-A-T

http://identifiers.org/hco/18/GRCh38#54937209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079237-A-C

54937209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079237-A-G

54937209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079237-A-T

http://identifiers.org/hco/18/GRCh38#54937210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079236-C-A

54937210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079236-C-T

54937276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079196-T-C

54937277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70079195-T-G

http://identifiers.org/hco/18/GRCh38#54937310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70079162-A-C

54937318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70079154-G-C

54937318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70079154-G-T

54937330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70079141-G-T

54937348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70079123-G-A

54937348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70079123-G-C

54937348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron variant
orthologous variants: 70079123-G-T

54937725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70077113-T-G

54937739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70077100-T-C

54937816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70077035-T-A

http://identifiers.org/hco/18/GRCh38#54937832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70077019-C-A

54937832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70077019-C-T

54937835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70077016-G-T

54937897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70076957-A-G

54937945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70076943-T-C

54938118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076774-T-C

54938138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076753-T-A

54938163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076728-A-G

http://identifiers.org/hco/18/GRCh38#54938187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70076707-C-A

54938205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076689-G-A

54938205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076689-G-T

http://identifiers.org/hco/18/GRCh38#54938249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70076648-C-A

54938249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076648-C-T

54938491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076397-C-T

54938492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076396-A-G

54938547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076337-A-G

54938569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076315-G-C

54938657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076229-G-T

54938697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70076193-A-G

54938935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70075961-T-C

54938998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70075897-G-A

54938998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70075897-G-C

54940283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70073958-A-T

54940471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70073765-A-G

54940471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70073765-A-T

54940561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70073675-C-T

http://identifiers.org/hco/18/GRCh38#54940671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70073597-C-A

54940954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70073321-A-G

54940954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70073321-A-T

http://identifiers.org/hco/18/GRCh38#54941048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70073204-C-A

54941048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70073204-C-T

54941085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 70073167-T-A

54941085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 70073167-T-C

54941085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 70073167-T-G

54942166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70072545-C-T

54942528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70072184-A-T

54942590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70072124-G-T

54942654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70072060-T-C

54942688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70072026-T-C

54942733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70071981-G-A

54942733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70071981-G-C

54945566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70069516-T-C

54945566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70069516-T-G

54946167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068852-T-C

54946169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068850-T-C

http://identifiers.org/hco/18/GRCh38#54946289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70068732-A-C

54946342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068687-A-G

54946485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068549-T-C

54946577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068483-C-T

54946607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068455-T-C

54946637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068426-T-A

54946644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068419-A-G

http://identifiers.org/hco/18/GRCh38#54946725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70068320-C-A

54946958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068082-T-C

54947092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067918-A-G

54947268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067744-C-G

54947312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067701-G-T

54947450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067576-A-T

54947633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067401-A-T

54947687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067352-A-G

54947908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067119-G-A

http://identifiers.org/hco/18/GRCh38#54948251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70066814-A-C

54950426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70066621-C-T

54950491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066559-G-C

54950568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066502-T-C

54950585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066482-T-C

54950605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066459-C-T

54950668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066387-T-A

54950668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066387-T-C

54950672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066383-T-C

54950683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066367-T-C

54950695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066355-C-T

54951390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70065485-T-C

54951653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70065205-A-G

54951738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70065131-G-A

54951751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70065118-T-C

54951787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70065081-G-A

54951889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70064984-A-G

54951962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70064910-G-T

54951977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70064895-T-C

54951995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70064879-T-C

http://identifiers.org/hco/18/GRCh38#54952003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70064871-C-A

54952051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70064823-C-T

54952079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70064806-T-C

54952493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70064310-T-C

54952643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70064164-T-C

54953170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70063775-G-A

54953259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70063707-T-A

http://identifiers.org/hco/18/GRCh38#54956682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70060992-C-A

54956686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70060988-T-C

54957053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70060654-T-C

54957074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70060633-T-A

54957096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70060615-C-G

54957822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70060085-T-C

54957875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70060040-T-G

54957878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70060037-A-G

54958246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059675-C-T

54958253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059668-A-G

54958388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059522-C-G

54958563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059343-G-T

http://identifiers.org/hco/18/GRCh38#54958577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70059332-C-A

54958618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059284-A-G

54958681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059233-T-G

http://identifiers.org/hco/18/GRCh38#54958702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#70059216-C-A

54958855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059120-C-G

54958856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059119-C-T

54958893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059099-T-G

54958968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70059049-C-T

54959061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70058956-A-T

54959198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70058814-C-T

54959240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70058768-G-A

54959245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70058763-C-T

http://identifiers.org/hco/18/GRCh38#54959297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#70058729-C-A

http://identifiers.org/hco/18/GRCh38#54959306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#70058720-C-A

54959359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 70058669-G-T

54959380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24350
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 70058648-C-T