18951082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61611720-C-T

18951172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61611640-G-A

18951240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61611585-G-A

18951299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61611521-G-C

18951500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61611355-T-A

18951500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61611355-T-C

18951500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61611355-T-G

http://identifiers.org/hco/17/GRCh38#18951632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61611261-C-A

18951632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61611261-C-T

http://identifiers.org/hco/17/GRCh38#18951726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61611197-C-A

18951804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61611132-G-T

18951817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61611119-A-G

18951817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61611119-A-T

18951836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61611103-G-A

http://identifiers.org/hco/17/GRCh38#18951854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61611087-C-A

http://identifiers.org/hco/17/GRCh38#18951917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61611049-A-C

18951917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61611049-A-G

18951919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61611047-T-A

http://identifiers.org/hco/17/GRCh38#18951983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61610992-A-C

18951983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610992-A-G

18951983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610992-A-T

18951985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610990-G-A

18951985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610990-G-C

18951985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610990-G-T

http://identifiers.org/hco/17/GRCh38#18951990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61610985-C-A

18951990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610985-C-T

http://identifiers.org/hco/17/GRCh38#18952132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61610841-C-A

18952132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610841-C-T

18952177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610798-T-C

18952241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 61610741-C-T

18952380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610625-C-G

18952380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61610625-C-T

18958667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61607155-T-C

18958727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 61607095-G-A

18958767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61607057-G-T

18958985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606761-A-G

18958998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606743-A-G

http://identifiers.org/hco/17/GRCh38#18959075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61606663-C-A

18959075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606663-C-G

18959075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606663-C-T

18959126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606615-C-G

18959126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606615-C-T

18959294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606445-G-A

18959294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606445-G-C

18959294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606445-G-T

18959338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606394-T-C

18959495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606257-T-C

18959503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606249-G-T

18959521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606231-T-A

18959528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606224-A-G

18959563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606188-G-A

18959622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61606129-G-A

18959622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61606129-G-T

18959694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61606060-G-A

http://identifiers.org/hco/17/GRCh38#18961209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61605458-A-C

18963750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61604046-T-C

18963860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61603928-G-A

18964061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61603724-C-T

18964127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61603649-G-A

18968925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61600651-T-G

http://identifiers.org/hco/17/GRCh38#18969025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61600544-C-A

18969025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61600544-C-G

18969025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61600544-C-T

18969061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 61600511-T-A

http://identifiers.org/hco/17/GRCh38#18969256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61600255-C-A

18969256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61600255-C-T

18969257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61600254-C-T

http://identifiers.org/hco/17/GRCh38#18969290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61600228-C-A

http://identifiers.org/hco/17/GRCh38#18969297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61600221-C-A

18969300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61600218-T-C

18969471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61600062-C-T

18969598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61600006-A-G

18969651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599975-G-A

18969651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599975-G-T

18969735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599918-T-C

18969735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599918-T-G

http://identifiers.org/hco/17/GRCh38#18969741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61599912-C-A

18969741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599912-C-T

18969919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599740-A-G

18970047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599631-T-C

http://identifiers.org/hco/17/GRCh38#18970170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61599564-C-A

18970451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599328-G-A

18970451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599328-G-T

http://identifiers.org/hco/17/GRCh38#18970464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61599310-C-A

18970526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599267-T-A

18970526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599267-T-C

18970532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599261-T-A

18970532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599261-T-C

18970718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599084-G-A

http://identifiers.org/hco/17/GRCh38#18970740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61599062-C-A

18970740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61599062-C-T

18970817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61598989-T-C

18970823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61598977-T-G

18971219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, splice_donor_variant
orthologous variants: 61598617-G-A

18971516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant
orthologous variants: 61598403-T-C

18971565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant
orthologous variants: 61598354-G-A

18971816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61598148-G-A

18971816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61598148-G-C

18971816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61598148-G-T

18971881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61598108-G-A

18971881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61598108-G-T

18971902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61598097-T-A

http://identifiers.org/hco/17/GRCh38#18972086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61597934-A-C

18972313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597737-T-C

18972314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597736-A-G

http://identifiers.org/hco/17/GRCh38#18972372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61597675-C-A

18972428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597629-G-A

18972428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597629-G-C

http://identifiers.org/hco/17/GRCh38#18972893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61597549-C-A

18972893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597549-C-G

18973235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597264-G-A

18973235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597264-G-T

18973258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597242-G-T

18973472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61597076-A-G

http://identifiers.org/hco/17/GRCh38#18976088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61595871-C-A

18976088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595871-C-G

18976225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595735-T-A

18976225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595735-T-G

18976315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595651-G-A

18976315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595651-G-T

http://identifiers.org/hco/17/GRCh38#18976434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61595550-C-A

18976434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595550-C-G

18976434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595550-C-T

http://identifiers.org/hco/17/GRCh38#18976500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61595493-A-C

http://identifiers.org/hco/17/GRCh38#18976594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61595426-C-A

http://identifiers.org/hco/17/GRCh38#18976602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61595418-C-A

18976602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595418-C-T

http://identifiers.org/hco/17/GRCh38#18976678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61595366-C-A

18976678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595366-C-G

18976678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595366-C-T

http://identifiers.org/hco/17/GRCh38#18976682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61595362-C-A

18976682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595362-C-T

18976748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595309-G-T

http://identifiers.org/hco/17/GRCh38#18976796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61595267-A-C

18976796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595267-A-T

18976819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595245-G-C

18976819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595245-G-T

18976839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595225-G-A

18976839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61595225-G-T

18977435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61594669-T-C

18977436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61594668-G-A

18977436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61594668-G-T

18977727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61594401-G-A

18977935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 61594196-A-G

http://identifiers.org/hco/17/GRCh38#18978104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61594027-C-A

http://identifiers.org/hco/17/GRCh38#18978111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61594020-C-A

18978111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61594020-C-T

http://identifiers.org/hco/17/GRCh38#18978210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61593921-C-A

18978210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61593921-C-T

18978244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 61593887-A-G

http://identifiers.org/hco/17/GRCh38#18978902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61593225-C-A

18978949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61593179-A-G

http://identifiers.org/hco/17/GRCh38#18979044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61593077-C-A

18979044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61593077-C-T

18979102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61593031-T-C

http://identifiers.org/hco/17/GRCh38#18979108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61593024-A-C

18979108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61593024-A-G

18979228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61592906-T-C

18979740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61592404-C-T

18980696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591905-A-G

18980733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591870-A-G

18980753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591858-G-A

18981181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591550-A-G

18981256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591485-A-G

18981281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591460-A-G

18981320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591452-G-A

18981456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591351-G-C

18981566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61591220-T-C

18981677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61591133-T-C

18981959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61590858-C-T

18981960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61590857-G-A

18982251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61590576-A-G

18984801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61589011-C-T

18984906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61588925-C-T

18985095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61588782-C-G

18985771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61587964-G-C

18985944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61587820-C-T

18986399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61587683-T-C

18986433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61587649-G-T

18986651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61587491-G-A

18986896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61587265-T-C

18987662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61586628-C-T

18988043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61586281-C-T

18988194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61586153-G-A

18988194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61586153-G-C

18988212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61586134-C-T

18988235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61586111-G-A

18988235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61586111-G-C

18988398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61585950-A-G

18988499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61585866-T-C

18988588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61585673-T-A

18988695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61585556-T-G

18988965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61585260-G-C

18989509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61584870-G-A

18989912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61584535-G-A

18989967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61584486-G-A

18990083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61584413-G-A

18990092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61584403-G-A

18990280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61584243-A-T

18990281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61584242-C-G

18990281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61584242-C-T

http://identifiers.org/hco/17/GRCh38#18990640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61583922-C-A

18991335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61583254-C-T

18992860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61583081-G-A

http://identifiers.org/hco/17/GRCh38#18992863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61583078-A-C

18993273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61582722-T-C

18994456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61582717-C-T

18994578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61582630-C-T

18994829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61582423-G-A

http://identifiers.org/hco/17/GRCh38#18995126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61582058-C-A

18995126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61582058-C-T

http://identifiers.org/hco/17/GRCh38#18995152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61582036-A-C

18995152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61582036-A-G

18995349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61581863-A-T

http://identifiers.org/hco/17/GRCh38#18996106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61581307-C-A

18996458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61581133-C-T

18996464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61581127-G-T

18996500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61581099-G-A

http://identifiers.org/hco/17/GRCh38#18996644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61580978-C-A

18996654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61580968-G-A

18996719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61580934-G-A

18996722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61580931-T-G

18997028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61580716-C-T

18997233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61580557-C-G

18997250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61580540-C-T

http://identifiers.org/hco/17/GRCh38#18998326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61580102-C-A

18999472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61579239-C-T

18999495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61579216-C-T

19000235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61578530-G-A

19000403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61578354-G-T

19000871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61577907-G-C

19000995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61577794-G-A

19001526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61577376-G-A

19001702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61577265-G-A

19001755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61577216-G-A

19002830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61576429-G-T

http://identifiers.org/hco/17/GRCh38#19003393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61575947-A-C

19003393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61575947-A-G

19003393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61575947-A-T

19003436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61575916-G-A

19003436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61575916-G-T

19004104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61575333-G-A

19004104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61575333-G-T

19004196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61575250-C-T

19004246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61575207-G-A

19004246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61575207-G-C

19004304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61575162-G-A

19004304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61575162-G-T

19004306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61575160-G-A

19004306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61575160-G-T

http://identifiers.org/hco/17/GRCh38#19004597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#61575032-C-A

19004597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: 61575032-C-T

19004687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: 61575007-G-C

19004687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: 61575007-G-T

http://identifiers.org/hco/17/GRCh38#19004796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#61574904-C-A

19004796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: 61574904-C-T

19004804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: 61574896-T-G

19004883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574821-G-A

19004883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574821-G-T

19004898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: 61574806-C-T

19005040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574769-C-T

http://identifiers.org/hco/17/GRCh38#19005042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61574767-C-A

19005042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574767-C-T

19005065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: 61574744-G-A

19005152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574682-G-A

19005167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574668-G-C

19005333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574514-G-T

19005412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574458-G-C

19005593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574304-C-T

19005842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61574037-C-T

19005886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61573997-G-A

19005886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61573997-G-T

19010225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61570855-A-G

19010290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61570790-G-A

19010746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61570482-G-T

19010759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61570469-A-G

http://identifiers.org/hco/17/GRCh38#19010782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61570445-C-A

19010832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61570395-G-A

19011044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61570165-A-G

19011314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61569946-G-A

19011346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, undefined
orthologous variants: 61569914-C-T

19011360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61569900-T-C

19013171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61569689-G-A

19013278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61569593-A-G

19013296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61569575-T-C

19013366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 61569519-T-G

19013378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 61569507-G-A

19013390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 61569497-A-G

19013651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61568108-G-T

19013663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61568097-T-C

19014041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61567776-A-G

19014082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61567746-G-A

http://identifiers.org/hco/17/GRCh38#19014673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61567365-A-C

19014697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61567343-G-A

19014697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61567343-G-C

19014702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61567340-A-G

19014762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61567275-C-G

19014762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61567275-C-T

19015129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61567021-C-G

19015168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61566982-T-G

19015227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566924-T-A

19015227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566924-T-C

19015227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566924-T-G

http://identifiers.org/hco/17/GRCh38#19015234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61566917-A-C

19015234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566917-A-G

19015234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566917-A-T

http://identifiers.org/hco/17/GRCh38#19015239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61566912-A-C

19015239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566912-A-G

19015239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566912-A-T

19016480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566513-A-G

19016535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566461-G-A

http://identifiers.org/hco/17/GRCh38#19016630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61566374-C-A

19016630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566374-C-T

19016887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61566171-G-A

19018009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61565691-G-T

19018028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61565676-C-T

http://identifiers.org/hco/17/GRCh38#19018133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61565571-C-A

http://identifiers.org/hco/17/GRCh38#19018138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61565564-A-C

19018138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61565564-A-G

19018169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61565535-G-A

http://identifiers.org/hco/17/GRCh38#19018224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61565474-C-A

19018224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61565474-C-T

19018269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61565434-G-T

19019451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61564793-A-G

http://identifiers.org/hco/17/GRCh38#19019559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61564685-C-A

19019559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 61564685-C-T

19019602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61564633-G-A

19019602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61564633-G-T

http://identifiers.org/hco/17/GRCh38#19019603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#61564632-C-A

19019603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61564632-C-T

19019671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61564589-C-T

19019734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61564544-G-A

19019734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61564544-G-T

19019752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61564526-G-A

19019752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61564526-G-T

19020011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61564229-A-G

http://identifiers.org/hco/17/GRCh38#19020102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61564158-C-A

http://identifiers.org/hco/17/GRCh38#19020114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61564146-C-A

19020114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: 61564146-C-T

http://identifiers.org/hco/17/GRCh38#19020306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61563954-C-A

19020329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: synonymous variant
orthologous variants: 61563931-T-C

19020363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61563897-C-G

19020363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61563897-C-T

19020364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61563896-G-A

19020364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: missense variant
orthologous variants: 61563896-G-C

19020498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563761-A-T

http://identifiers.org/hco/17/GRCh38#19020532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61563729-C-A

19020532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563729-C-T

http://identifiers.org/hco/17/GRCh38#19020634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61563646-A-C

19020643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563634-A-T

19020682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563606-G-A

http://identifiers.org/hco/17/GRCh38#19020803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61563493-C-A

19020842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563451-A-G

19020842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563451-A-T

19020936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563349-T-C

http://identifiers.org/hco/17/GRCh38#19020951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61563321-A-C

http://identifiers.org/hco/17/GRCh38#19020979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61563294-C-A

19020979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563294-C-T

19021112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563217-G-A

19021112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563217-G-T

19021129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563206-T-C

19021158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563189-T-C

http://identifiers.org/hco/17/GRCh38#19021224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61563125-A-C

19021294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563081-A-G

19021380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563028-G-A

19021380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61563028-G-T

http://identifiers.org/hco/17/GRCh38#19021481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61562969-C-A

19021481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562969-C-G

19021481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562969-C-T

19021522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562928-G-A

19021555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562917-G-A

19021676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562841-G-T

http://identifiers.org/hco/17/GRCh38#19021698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#61562828-C-A

19021698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562828-C-T

19021728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562800-G-A

19021728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562800-G-T

19021747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3 prime UTR variant
orthologous variants: 61562781-A-G

19021897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 61562704-T-C

http://identifiers.org/hco/17/GRCh38#19022005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#61562636-C-A

19022005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 61562636-C-T

http://identifiers.org/hco/17/GRCh38#19022017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#61562624-C-A

19022017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 61562624-C-T

19022307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61562346-C-T

19022500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61562249-G-A

19022500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23155
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61562249-G-C