http://identifiers.org/hco/3/GRCh38#101828035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55658972-C-A

101828035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55658972-C-T

101828078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55658929-T-C

101828604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55657961-A-G

101828661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55657903-C-G

101828845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55657718-C-T

101829254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, undefined
orthologous variants: 55657085-G-C

101829276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, undefined
orthologous variants: 55657063-G-A

101829308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55657041-G-A

101829596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55656770-T-C

http://identifiers.org/hco/3/GRCh38#101829627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55656739-C-A

101829643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55656724-G-T

101829648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55656719-T-C

101829697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55656674-G-T

http://identifiers.org/hco/3/GRCh38#101829721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55656654-A-C

101829957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55656451-A-T

101830050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55656360-C-T

101830051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55656359-A-G

101831091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55655380-G-A

101831165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55655310-A-G

101831258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55655187-G-T

101831271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55655174-A-G

101831545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55654910-G-A

101832953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55653965-C-T

101832969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55653949-G-C

101833112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55653814-A-G

101833193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55653726-C-T

101833419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55653500-A-G

101833860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55653063-T-C

101834656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55652564-C-G

101834656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55652564-C-T

101834744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55652464-A-G

101834887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55652331-G-A

101835104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55652134-A-G

101835340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55651902-T-G

101836356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55649143-C-T

101836424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55649093-A-G

101836435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55649083-C-T

101836524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55649002-A-G

101836602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55648923-A-G

101837433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55648136-T-G

101837529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55648083-A-G

http://identifiers.org/hco/3/GRCh38#101837538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55648074-C-A

101837753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55647882-G-A

101837765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55647871-A-G

101837905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55647737-G-C

101837952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55647692-T-C

http://identifiers.org/hco/3/GRCh38#101847985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55643929-C-A

101847985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643929-C-G

101847985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643929-C-T

101847992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643922-A-G

101847999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643915-G-A

101847999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643915-G-C

101848072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643838-G-C

101848203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643727-G-A

101848395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643563-C-G

101848549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643430-A-G

http://identifiers.org/hco/3/GRCh38#101848580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55643364-C-A

101848610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643307-T-A

101848610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643307-T-C

http://identifiers.org/hco/3/GRCh38#101848707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55643200-A-C

101848766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55643137-G-T

http://identifiers.org/hco/3/GRCh38#101848898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#55642993-A-C

101848983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642922-T-C

http://identifiers.org/hco/3/GRCh38#101849088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55642880-C-A

101849088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642880-C-T

http://identifiers.org/hco/3/GRCh38#101849127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55642867-C-A

101849127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642867-C-T

http://identifiers.org/hco/3/GRCh38#101849165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#55642830-C-A

101849165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 55642830-C-T

101849222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642785-G-A

101849222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642785-G-T

101849229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642772-G-A

101849229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642772-G-T

101849238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 55642757-G-C

101849238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 55642757-G-T

http://identifiers.org/hco/3/GRCh38#101849239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#55642756-A-C

101849239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 55642756-A-G

101849259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642726-G-A

101849259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642726-G-C

http://identifiers.org/hco/3/GRCh38#101849365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#55642635-C-A

101849365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 55642635-C-T

http://identifiers.org/hco/3/GRCh38#101849479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55642532-C-A

101849479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642532-C-G

101849479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642532-C-T

101849516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642495-A-G

101849516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55642495-A-T

101849592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642452-G-A

101849592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642452-G-C

101849592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642452-G-T

101849719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55642324-A-G

101849743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642300-T-C

101849743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642300-T-G

101849758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642285-G-A

101849758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642285-G-C

101849758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642285-G-T

101849842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642204-T-A

101849842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55642204-T-C

101849854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55642192-G-A

101849854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55642192-G-T

101849968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55642076-G-A

101849968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55642076-G-T

101850030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641989-A-G

101850032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641987-G-A

101850049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641971-T-A

101850049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641971-T-G

http://identifiers.org/hco/3/GRCh38#101850058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55641965-C-A

101850058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641965-C-T

101850136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641853-T-A

101850136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641853-T-C

101850136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641853-T-G

101850195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641807-A-T

101850210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641792-A-G

101850243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641762-T-G

101850316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55641684-G-T

http://identifiers.org/hco/3/GRCh38#101850472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55641534-C-A

101850472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641534-C-T

101850908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641109-A-G

101850936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55641077-C-T

101851095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640911-C-T

101851128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640882-T-C

101851167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640847-C-T

101851181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640833-G-A

101851471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640620-A-G

101851663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640449-G-A

http://identifiers.org/hco/3/GRCh38#101851946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55640220-C-A

101851946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640220-C-T

101851972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640178-A-G

101852041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55640103-T-C

http://identifiers.org/hco/3/GRCh38#101852180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55639972-A-C

101852209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55639943-T-G

101852233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55639919-T-C

101852274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55639885-T-C

http://identifiers.org/hco/3/GRCh38#101852296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55639858-C-A

http://identifiers.org/hco/3/GRCh38#101852351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55639811-C-A

101852568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55639578-G-A

101852700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55639420-T-C

101852703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55639417-T-A

101852703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55639417-T-C

101852703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55639417-T-G

101852718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55639402-G-A

101852718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55639402-G-T

101852863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55639238-A-G

101853074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55638921-A-G

101853075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55638911-T-C

101853304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: 55638685-G-A

101853304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: 55638685-G-T

101853423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55638566-G-A

101853445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: 55638514-A-G

101853445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: 55638514-A-T

101853493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: 55638466-G-C

101853532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: 55638427-C-T

http://identifiers.org/hco/3/GRCh38#101853565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55638394-C-A

101853565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: 55638394-C-G

101853574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, missense_variant
orthologous variants: 55638385-T-C

101853693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: synonymous variant
orthologous variants: 55638263-G-A

101853724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: missense variant
orthologous variants: 55638232-C-T

101853954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55638053-T-A

101853954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55638053-T-C

101855026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55636862-T-A

101855026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55636862-T-C

101855077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55636809-G-T

101855211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55636675-A-G

101855282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55636608-A-G

101855317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55636572-T-A

101855341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55636545-T-C

101855597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636296-T-C

101855597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636296-T-G

101855625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636268-G-A

101855625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636268-G-C

101855625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636268-G-T

101855631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636262-T-G

101855640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636254-A-T

101855691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636209-G-T

101855692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55636208-A-G

101855744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55636159-C-T

101855852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55636051-G-A

101855919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635984-G-A

101855929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635975-G-C

101855998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635894-T-C

101856022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55635847-G-A

101856022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55635847-G-T

101856627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron variant
orthologous variants: 55635381-A-T

http://identifiers.org/hco/3/GRCh38#101856765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55635245-C-A

101856765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635245-C-T

101856879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635139-A-G

http://identifiers.org/hco/3/GRCh38#101856895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55635123-A-C

101856952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635070-A-G

101856952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635070-A-T

101856962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635060-G-A

101856962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635060-G-C

101856962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635060-G-T

http://identifiers.org/hco/3/GRCh38#101856968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55635055-C-A

101856968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55635055-C-G

101857050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55634734-T-C

101857261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55634511-G-A

101857261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55634511-G-C

101857270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55634501-T-C

101857280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55634491-C-T

101857445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55634325-C-T

101857564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55634206-G-T

101857897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55634143-T-C

101857897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55634143-T-G

101858031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55634044-A-G

101858043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55634032-A-T

101858056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55634013-T-G

101858141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633934-T-C

101858176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633898-A-G

101858348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633770-T-C

101858364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633754-G-A

101858386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633736-A-G

101858422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633703-C-T

101858438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633687-G-T

101858474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633653-T-A

101858504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633623-T-C

101858641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633496-C-T

101858663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633465-A-G

101858718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633419-G-A

101858772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633364-T-A

http://identifiers.org/hco/3/GRCh38#101859292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55633164-A-C

101859292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55633164-A-G

101859817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55632603-C-T

http://identifiers.org/hco/3/GRCh38#101859832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55632588-A-C

101859896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55632530-G-A

101859921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55632505-T-C

101859921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55632505-T-G

101860723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55632030-C-G

101860882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55631884-G-T

101860906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55631863-G-A

101860908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55631861-A-G

101860938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29805
most severe consequence: 3 prime UTR variant
orthologous variants: 55631829-C-G