http://identifiers.org/hco/12/GRCh38#1820318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119307858-C-A

1820318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307858-C-G

1820322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307854-G-T

http://identifiers.org/hco/12/GRCh38#1820476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119307748-C-A

1820493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307730-G-A

1820493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307730-G-T

http://identifiers.org/hco/12/GRCh38#1820494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119307729-C-A

1820494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307729-C-T

1820552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307671-T-C

http://identifiers.org/hco/12/GRCh38#1820714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119307514-C-A

1820714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307514-C-G

1820836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307432-G-A

http://identifiers.org/hco/12/GRCh38#1820906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119307376-C-A

1820906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119307376-C-T

1821737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306595-T-C

1821968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306370-G-A

1821968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306370-G-T

1821971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306368-G-A

1821971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306368-G-T

1821972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306367-A-G

http://identifiers.org/hco/12/GRCh38#1822058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119306283-C-A

1822149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 119306202-G-T

1822161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306190-A-T

http://identifiers.org/hco/12/GRCh38#1822164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119306187-C-A

1822164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306187-C-T

1822278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306067-G-A

1822278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119306067-G-T

1822406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305931-C-T

1822732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305579-T-C

http://identifiers.org/hco/12/GRCh38#1822805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119305493-C-A

1822805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305493-C-T

1822913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305416-C-T

1822968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305370-G-A

1823044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305316-C-T

1823256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305150-G-A

1823256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305150-G-T

1823265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305141-C-T

1823293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305108-G-A

1823310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305092-G-A

1823310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305092-G-T

1823379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305029-T-C

1823383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119305025-G-A

http://identifiers.org/hco/12/GRCh38#1823387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119305021-C-A

1823511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119304927-C-G

1823542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119304899-G-A

1823885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119304675-C-G

1823885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119304675-C-T

1824144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119304368-C-T

1824338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119304115-A-G

1824361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119304093-A-G

1824631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303844-C-G

1824631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303844-C-T

1824950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303571-G-A

1824950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303571-G-C

1824981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303550-G-A

1825242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303398-G-A

1825246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303394-G-C

1825395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303301-C-G

1825395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119303301-C-T

1825688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302999-G-A

1825891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302808-G-C

1825905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302794-T-G

1826010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302687-G-A

1826012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302685-G-A

1826238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302505-G-C

1826268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302479-C-G

1826398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302380-G-C

http://identifiers.org/hco/12/GRCh38#1826584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119302236-C-A

1826584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302236-C-G

1826752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119302061-C-T

1826903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301780-T-A

1826904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301779-C-T

1827002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301702-A-T

http://identifiers.org/hco/12/GRCh38#1827318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119301433-C-A

1827318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301433-C-G

1827318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301433-C-T

http://identifiers.org/hco/12/GRCh38#1827384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119301364-C-A

1827384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301364-C-T

1827385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301363-T-A

1827385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301363-T-C

1827404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 119301348-T-A

1827404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 119301348-T-C

1827434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301319-T-C

http://identifiers.org/hco/12/GRCh38#1827542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119301219-C-A

1827542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301219-C-G

1827557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301204-G-A

1827557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301204-G-C

http://identifiers.org/hco/12/GRCh38#1827561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119301200-C-A

1827561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301200-C-G

1827561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301200-C-T

http://identifiers.org/hco/12/GRCh38#1827569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119301185-C-A

1827660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301096-G-A

http://identifiers.org/hco/12/GRCh38#1827691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119301073-C-A

1827691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119301073-C-T

1827947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300839-G-A

1827947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300839-G-T

1827975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300823-G-A

1827975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300823-G-C

1827975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300823-G-T

1827983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119300815-G-A

1827983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300815-G-T

http://identifiers.org/hco/12/GRCh38#1828010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119300787-C-A

1828010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119300787-C-T

1828025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119300772-T-A

1828025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119300772-T-C

1828033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300764-G-A

1828033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300764-G-T

1828034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119300763-G-A

1828034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119300763-G-C

1828034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119300763-G-T

http://identifiers.org/hco/12/GRCh38#1828035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119300762-C-A

1828035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300762-C-T

http://identifiers.org/hco/12/GRCh38#1828063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119300749-C-A

1828063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300749-C-T

http://identifiers.org/hco/12/GRCh38#1828067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119300745-C-A

1828067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119300745-C-T

1828236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300587-G-A

1828236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300587-G-C

1828236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300587-G-T

1828240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300583-G-A

1828240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300583-G-C

1828240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300583-G-T

1828243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300580-G-A

1828243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300580-G-C

1828243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300580-G-T

1828245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300578-T-A

1828245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300578-T-C

1828245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300578-T-G

1828334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300537-T-C

1828334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300537-T-G

http://identifiers.org/hco/12/GRCh38#1828348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119300524-C-A

1828421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300468-G-A

1828459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300436-G-A

1828609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300287-T-C

1828692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300202-C-T

http://identifiers.org/hco/12/GRCh38#1828801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119300091-C-A

1828858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300063-C-T

1828930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119300014-C-T

1828957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119299987-C-T

1829086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119299864-T-C

1829169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119299764-G-A

1829701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298980-C-T

1829753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298936-G-A

http://identifiers.org/hco/12/GRCh38#1829767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119298924-A-C

1830009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298740-G-C

1830011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298736-C-T

1830131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298620-A-G

1830302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298471-G-A

1830587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298242-A-G

1830845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298049-G-A

1830845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298049-G-T

http://identifiers.org/hco/12/GRCh38#1830857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119298037-C-A

1830857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298037-C-T

1830879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119298017-A-G

1830908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297997-T-C

1830919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297986-T-C

1830937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 119297968-A-T

1830971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297934-C-T

1831138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297767-C-T

1831378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297527-C-T

1831489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297416-G-C

1831489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297416-G-T

1831878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297156-C-T

1832006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119297038-A-T

1832410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119295965-C-T

1832423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119295952-G-A

1832563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119295808-T-A

1832900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119295473-C-G

1833287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119295188-T-A

1833572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119295051-G-C

1833607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119295031-C-T

1833654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119295008-C-T

1833723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294968-G-A

1833723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294968-G-T

1833735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294953-C-T

1833743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294945-G-A

1833989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294715-G-A

1834146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294590-T-C

1834163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294573-A-G

1834198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294538-T-A

1834198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294538-T-C

1834230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294506-T-C

http://identifiers.org/hco/12/GRCh38#1834241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#119294495-C-A

1834249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294487-T-C

1834262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 119294474-T-C

1834548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294188-G-T

http://identifiers.org/hco/12/GRCh38#1834723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119294013-C-A

1834723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119294013-C-T

http://identifiers.org/hco/12/GRCh38#1834788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119293929-C-A

1834788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293929-C-T

1834798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293919-C-T

http://identifiers.org/hco/12/GRCh38#1834799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119293918-C-A

1834799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293918-C-G

1834799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293918-C-T

1834913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293840-G-A

1834913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293840-G-T

1835002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293754-T-A

http://identifiers.org/hco/12/GRCh38#1835065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119293701-C-A

1835370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293392-A-G

http://identifiers.org/hco/12/GRCh38#1835450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119293282-C-A

1835450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293282-C-G

1835450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293282-C-T

http://identifiers.org/hco/12/GRCh38#1835536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119293207-C-A

1835536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293207-C-T

http://identifiers.org/hco/12/GRCh38#1835544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119293199-C-A

http://identifiers.org/hco/12/GRCh38#1835584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119293160-C-A

1835691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293059-T-C

1835726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293046-G-A

1835726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293046-G-T

1835739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119293033-G-A

1835794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292982-G-A

1835821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292955-G-A

1835821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292955-G-C

1835821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292955-G-T

1835822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292954-C-T

1835845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292935-T-C

http://identifiers.org/hco/12/GRCh38#1835915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119292875-C-A

http://identifiers.org/hco/12/GRCh38#1836001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119292796-C-A

http://identifiers.org/hco/12/GRCh38#1836014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119292784-C-A

1836015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292783-T-C

1836021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292777-C-T

1836101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292695-G-A

1836218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292569-T-A

1836218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292569-T-C

http://identifiers.org/hco/12/GRCh38#1836241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119292547-C-A

1836241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292547-C-G

1836313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292501-T-C

1836314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292500-G-A

http://identifiers.org/hco/12/GRCh38#1836434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
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/6/GRCm39#119292390-C-A

1836434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292390-C-T

1836479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292354-G-C

1836479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32443
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119292354-G-T