94324543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 38768404-C-G

94332253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38775266-C-G

94332523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38775518-G-A

94332574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38775575-T-C

94332576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38775577-T-A

http://identifiers.org/hco/10/GRCh38#94333428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38776902-C-A

http://identifiers.org/hco/10/GRCh38#94334076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38777922-C-A

http://identifiers.org/hco/10/GRCh38#94334091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38777937-A-C

http://identifiers.org/hco/10/GRCh38#94334092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38777938-A-C

94334092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38777938-A-G

94334175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38778011-T-C

94334258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38778094-C-G

94334368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778201-G-A

94334368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778201-G-C

94334368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778201-G-T

94334451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778443-T-C

http://identifiers.org/hco/10/GRCh38#94334564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38778634-C-A

94334564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778634-C-T

94334570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778642-T-A

94334570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778642-T-G

94334589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778668-T-C

94334667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38778765-A-G

94334681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38778779-C-G

94334681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38778779-C-T

94334757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778856-A-G

94334757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778856-A-T

94334758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778857-T-A

http://identifiers.org/hco/10/GRCh38#94334782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38778881-A-C

94334782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778881-A-G

94337759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38781127-G-A

94337759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38781127-G-T

94337953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38781319-T-A

94338050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782030-T-C

94338158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782120-T-C

94338220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782161-G-A

94338250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782194-G-C

94338294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782248-A-G

94338459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782378-T-G

94338552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782459-G-A

94338552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782459-G-C

94338552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782459-G-T

94338561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782468-T-C

http://identifiers.org/hco/10/GRCh38#94338599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38782540-C-A

94338599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782540-C-T

94339701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783378-A-G

94339701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783378-A-T

94339936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783608-T-C

94339936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783608-T-G

94339979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783650-G-T

http://identifiers.org/hco/10/GRCh38#94340028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38783697-C-A

94340028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783697-C-T

94340029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783698-A-G

94340081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783737-A-G

http://identifiers.org/hco/10/GRCh38#94340124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38783785-A-C

94340178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783837-G-C

94340178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783837-G-T

94340201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783859-G-T

94340224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783880-T-C

94340294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38783948-G-C

94340514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784163-G-A

94340514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784163-G-C

94340514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784163-G-T

94340515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784164-G-A

94340515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784164-G-T

http://identifiers.org/hco/10/GRCh38#94340540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38784186-A-C

94341758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784326-A-G

94341771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784341-A-G

94341771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784341-A-T

94341857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784879-G-T

94341879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784902-T-A

94341879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784902-T-C

94341879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784902-T-G

http://identifiers.org/hco/10/GRCh38#94343880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38786691-A-C

94343880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38786691-A-G

94343900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38786710-T-C

94343914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38786723-C-T

94343989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38786775-A-G

94344098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38786885-T-C

94344272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787142-A-G

94344319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787223-T-A

94344319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787223-T-C

94344319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787223-T-G

94344533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787460-C-T

94344564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787490-T-A

94344660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787579-A-G

94344663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787582-G-T

94344736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787651-C-T

http://identifiers.org/hco/10/GRCh38#94344761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38787676-C-A

94344877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38787778-C-G

94344877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38787778-C-T

94344880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38787781-T-C

94344981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787956-T-A

http://identifiers.org/hco/10/GRCh38#94344990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38787974-C-A

94344990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787974-C-T

94345011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38787991-T-C

94345060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38788035-A-G

http://identifiers.org/hco/10/GRCh38#94346286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38792727-A-C

94346286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792727-A-T

94346287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792728-G-T

http://identifiers.org/hco/10/GRCh38#94346298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38792743-C-A

94346319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792762-T-A

94346375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792793-A-G

94346390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792809-A-G

http://identifiers.org/hco/10/GRCh38#94346404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38792822-A-C

94346404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792822-A-G

94346418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38792836-G-A

94346440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38792858-T-C

94347403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38793528-A-G

94347405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38793531-G-A

94347405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38793531-G-T

94348844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38795188-A-T

94348951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38795281-T-A

94349203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38795485-C-T

http://identifiers.org/hco/10/GRCh38#94349218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38795500-A-C

http://identifiers.org/hco/10/GRCh38#94349237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38795518-A-C

94349286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38795567-A-T

94350062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38795899-T-C

94350077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38795914-T-G

94350114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 38795971-A-G

http://identifiers.org/hco/10/GRCh38#94350257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38796114-A-C

94350257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38796114-A-G

http://identifiers.org/hco/10/GRCh38#94352445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38798579-C-A

94352445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798579-C-T

http://identifiers.org/hco/10/GRCh38#94352525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38798609-C-A

94352525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798609-C-T

http://identifiers.org/hco/10/GRCh38#94352844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38798697-C-A

94352844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798697-C-T

94353106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798952-T-A

94353106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798952-T-C

94353124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798970-G-A

94353124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798970-G-T

94353148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798973-G-A

94353148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798973-G-T

94353167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38798992-A-G

94354257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799703-T-C

http://identifiers.org/hco/10/GRCh38#94354430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38799851-C-A

94354430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799851-C-T

94354446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799867-C-G

94354447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799868-C-T

94354461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799882-G-C

94354466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799887-T-C

94354502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799904-A-G

94354517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799919-T-G

94354521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799923-C-T

94354611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38800191-T-A

94354871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38800720-A-G

94354871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38800720-A-T

94354875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38800724-T-C

94355044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38800869-A-G

94355073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38800898-G-C

94355073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38800898-G-T

94355195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801017-A-G

http://identifiers.org/hco/10/GRCh38#94355213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38801034-C-A

94355213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801034-C-T

94355233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801054-A-G

http://identifiers.org/hco/10/GRCh38#94355234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38801055-A-C

94355234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801055-A-G

http://identifiers.org/hco/10/GRCh38#94355236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38801065-A-C

94355236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801065-A-G

94355525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801329-A-T

94355999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801799-A-T

94356001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801801-C-T

94356025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801835-T-C

http://identifiers.org/hco/10/GRCh38#94356083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38801899-C-A

94356147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801967-T-G

94356194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802008-G-A

94356284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802253-C-T

94356395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802392-G-A

94356399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802396-A-G

94356452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802436-G-C

94356452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802436-G-T

http://identifiers.org/hco/10/GRCh38#94356469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38802453-A-C

94356583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38802570-T-C

94356588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38802575-G-A

94356588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38802575-G-T

94356638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802623-G-T

94356663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802652-A-G

94356666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802655-T-G

94356724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802695-T-G

94356738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802712-G-A

94356738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802712-G-T

94356977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802921-A-G

http://identifiers.org/hco/10/GRCh38#94357037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38802978-A-C

94357037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38802978-A-G

94357132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38803076-G-A

94357132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38803076-G-T

94357135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38803088-G-A

94357135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38803088-G-T

94357166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38803122-A-G

94357168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38803124-A-G

94357189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38803145-T-C

94357196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38803152-G-A

94357196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38803152-G-T

94357202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38803158-A-G

94357247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38803203-T-C

http://identifiers.org/hco/10/GRCh38#94357483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38803414-C-A

94357483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38803414-C-G

94357483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38803414-C-T

http://identifiers.org/hco/10/GRCh38#94357497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38803429-A-C

94357514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38803447-G-A

94357514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38803447-G-C

http://identifiers.org/hco/10/GRCh38#94357988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38803893-C-A

94357988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38803893-C-T

http://identifiers.org/hco/10/GRCh38#94358011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38803962-C-A

94358011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38803962-C-T

http://identifiers.org/hco/10/GRCh38#94358091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38804035-A-C

http://identifiers.org/hco/10/GRCh38#94358154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38804098-A-C

94358190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38804134-C-G

94358190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38804134-C-T

94358218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38804162-G-A

94358218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38804162-G-T

http://identifiers.org/hco/10/GRCh38#94358240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38804173-A-C

http://identifiers.org/hco/10/GRCh38#94358327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38804227-C-A

94358327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38804227-C-G

http://identifiers.org/hco/10/GRCh38#94358333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38804233-C-A

http://identifiers.org/hco/10/GRCh38#94358428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38804265-C-A

94358656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38804412-C-G

94358835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38804580-C-G

94361141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805909-T-C

94361221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805985-T-C

94361322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806089-A-T

94361361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38806128-C-T

94361443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38806200-T-A

94361587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806327-G-T

94361671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 38806388-G-A

94361891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806611-A-G

94361957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806681-G-C

94361958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806682-A-G

94361990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806709-C-T

94362060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806783-A-T

94362066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806789-T-A

94362066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806789-T-C

http://identifiers.org/hco/10/GRCh38#94362067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38806790-C-A

94362067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38806790-C-T

94362523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38807211-G-T

94362647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38807326-G-C

94362697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38807390-A-T

94362699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38807403-T-C

94362699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38807403-T-G

94362715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38807418-T-A

94362715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38807418-T-C

94362798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38807505-G-A

http://identifiers.org/hco/10/GRCh38#94362925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24034
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#38807631-A-C