24270820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75047888-C-G

24270820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75047888-C-T

24270823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75047891-A-G

http://identifiers.org/hco/22/GRCh38#24270894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75047963-C-A

24270894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75047963-C-T

24271435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75048453-C-T

24271449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048455-C-T

http://identifiers.org/hco/22/GRCh38#24271497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75048500-C-A

24271982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049145-T-A

24273197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049950-C-G

24273197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049950-C-T

24273435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75050853-G-A

24284774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057844-A-G

24284981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75058025-A-G

24285173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75058163-T-C

24285200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75058190-C-G

24285316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75058305-C-T

24289402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75059403-G-T

http://identifiers.org/hco/22/GRCh38#24289460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75059514-A-C

24289979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75060069-T-G

24290127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75060201-C-G

http://identifiers.org/hco/22/GRCh38#24290609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75060593-C-A

24290609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75060593-C-T

24290939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75061371-C-G

24291016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75061437-T-A

24291910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063167-G-A

24292148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063348-A-G

24302103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066421-G-T

24302149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066466-T-C

http://identifiers.org/hco/22/GRCh38#24302156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75066473-C-A

24302156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066473-C-T

24302172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066489-G-A

24302172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066489-G-T

24302462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066780-G-A

24302462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066780-G-T

24302532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066848-G-A

24302532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066848-G-T

24302579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066894-A-G

24303538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75068803-T-G

24303598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068862-A-T

24303987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069687-T-G

24304076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069842-A-G

24304142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069948-A-G

24304183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069987-A-T

24304210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070014-A-G

24304354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070134-T-C

http://identifiers.org/hco/22/GRCh38#24304394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75070167-C-A

24304394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070167-C-G

24304396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75070169-G-T

24304412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75070187-G-A

24304412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75070187-G-T

24304450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75070214-A-T

24304466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070231-A-G

24304471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070236-A-G

24304680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070387-C-G

24304950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070820-G-A

24305131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75071015-G-T

24305289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75071162-A-G

24310819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75073811-T-C

24311005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75073985-C-G

24311038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75074018-C-G

24311096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75074073-C-T

http://identifiers.org/hco/22/GRCh38#24311552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75074515-C-A

24311887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75074859-A-G

http://identifiers.org/hco/22/GRCh38#24311951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75074924-A-C

24311951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75074924-A-T

24312540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076098-T-C

24312540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076098-T-G

24312556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076116-A-G

24313037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076626-T-C

24313068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076657-G-C

http://identifiers.org/hco/22/GRCh38#24313185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75076779-C-A

24313277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076863-T-G

24313373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75076959-G-A

24315406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077323-G-T

24315670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077589-A-G

24316087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75078273-C-T

24316187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75078372-T-G

24319627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75079301-A-G

24319683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75079348-T-C

24319695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75079360-A-T

24320852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75080467-A-G

24320852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75080467-A-T

24320857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75080472-C-T

24321502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75081127-G-C

24321670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081298-T-C

http://identifiers.org/hco/22/GRCh38#24321877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75081505-C-A

24321877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081505-C-T

http://identifiers.org/hco/22/GRCh38#24321943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75081571-A-C

24321943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081571-A-G

24321956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75081584-T-A

24321956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75081584-T-G

24322036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081664-C-T

24322072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081700-T-C

24322105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081733-C-G

24322105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081733-C-T

24322234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081862-G-A

24322234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081862-G-C

24322234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75081862-G-T

24322486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75082114-C-T

http://identifiers.org/hco/22/GRCh38#24322516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75082144-C-A

http://identifiers.org/hco/22/GRCh38#24322968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75082592-A-C

24322968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082592-A-G

http://identifiers.org/hco/22/GRCh38#24323018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75082615-A-C

24323018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082615-A-G

24323059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082652-T-C

24323103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082689-A-G

24323115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082701-C-G

24323115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082701-C-T

24323129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082715-G-C

24323129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082715-G-T

24323153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082732-G-A

24323164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082743-G-A

24323301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082856-A-G

24323535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75083074-A-G

24323894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75083968-T-C

http://identifiers.org/hco/22/GRCh38#24324121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75084191-A-C

24324133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75084203-C-G

24324133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75084203-C-T

24325085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090992-T-G

24325114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75091021-T-C

24328419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093319-T-C

24328970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093828-C-T

24329043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093878-G-T

24329397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093984-A-T

24329631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094197-T-C

http://identifiers.org/hco/22/GRCh38#24330142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75094693-A-C

24330142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094693-A-G

24330448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094994-C-G

24330448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094994-C-T

24330651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095049-T-G

http://identifiers.org/hco/22/GRCh38#24331085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75095395-A-C

24331098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095408-T-C

24331123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095433-T-G

24331639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095932-G-A

http://identifiers.org/hco/22/GRCh38#24331675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75095953-C-A

24331782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75096056-A-G

24331829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75096095-A-T

24331921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75096195-T-C

24333736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75097243-A-G

24334716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75097943-G-A

24334716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75097943-G-C

24334823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75098076-A-G

24334823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75098076-A-T

24334995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75098240-G-A

24335084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75098326-T-C

24338526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75099252-G-C

24338594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75099313-G-A

24338594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75099313-G-T

24338636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75099355-T-C

24339746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75100067-G-A

24340446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75100144-T-C

24341503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75100881-A-G

24342003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75101390-C-T

24346430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75102628-G-A

24346569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75102764-A-G

24346674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75102847-A-G

24346913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75103167-T-A

http://identifiers.org/hco/22/GRCh38#24346972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75103222-C-A

24346972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75103222-C-T

24346977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75103227-T-C

24347000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75103249-T-A

24347000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75103249-T-C

http://identifiers.org/hco/22/GRCh38#24347045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75103299-C-A

24347045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75103299-C-T

24347273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75103511-A-G

http://identifiers.org/hco/22/GRCh38#24360180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75105820-C-A

24361969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108740-C-T

24362178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108990-G-A

24362491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109155-C-T

24362689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109300-G-A

24363168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109764-G-A

24363168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109764-G-T

24363182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109778-A-G

24363182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109778-A-T

24363218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109814-C-T

http://identifiers.org/hco/22/GRCh38#24363231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75109824-C-A

24363249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109839-T-C

24363292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75109882-G-T

24365448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112579-T-C

24365453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112584-T-C

24365458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112589-A-G

24365677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112791-G-A

24365705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112818-T-A

24365705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112818-T-G

24369114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115588-T-C

http://identifiers.org/hco/22/GRCh38#24369170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75115646-C-A

24369189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115658-T-C

24369383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115856-G-T

http://identifiers.org/hco/22/GRCh38#24369866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75116542-A-C

24370041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75116687-A-G

24370110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75116742-T-C

24380268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75119067-G-A

http://identifiers.org/hco/22/GRCh38#24380302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75119100-C-A

24380375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75119175-A-G

24389642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124444-A-T

http://identifiers.org/hco/22/GRCh38#24389780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75124571-A-C

24389817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124607-G-A

24389965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124663-T-G

24390040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124743-T-C

24390193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124852-G-A

24390226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124888-C-T

24390239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124910-G-A

24390241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124912-C-T

24390456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75125047-A-T

24391946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75126258-T-G

24392011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75126350-A-G

http://identifiers.org/hco/22/GRCh38#24392143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75126755-A-C

http://identifiers.org/hco/22/GRCh38#24393375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75127908-A-C

24393375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127908-A-G

24393640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128406-C-G

24393640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128406-C-T

24393845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128576-C-G

24393845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128576-C-T

24393912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128634-G-A

24394123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128811-G-T

http://identifiers.org/hco/22/GRCh38#24394595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75129299-A-C

24394690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129390-C-T

24394836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129491-T-G

24395157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129684-T-G

24395236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129754-G-A

24395263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129771-A-G

24395367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129884-A-G

http://identifiers.org/hco/22/GRCh38#24395584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75130086-A-C

24396208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130376-T-C

24396638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130481-C-G

24396642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130485-G-C

24396899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130701-T-A

24397274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130995-C-T

24397357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75131078-T-C

24399133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75132996-C-T

24399262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75133129-G-A

24400378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75133790-T-C

24400696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134087-G-A

24400748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134162-C-T

24400827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134243-C-T

24401102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134471-C-T

24401166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134520-G-A

24401231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134587-C-T

24401434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134753-T-C

24401434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134753-T-G

24401562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134861-C-G

24401907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75135105-G-T

24402415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75135601-C-T

24405957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75139245-G-A

24406139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75139442-G-A

24406161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75139471-A-G

24406752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75139801-C-T

24406906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75139967-T-C

24407069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75140118-A-G

24407458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75140407-G-A

24407843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75140818-C-T

24408170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75141092-T-C

24408224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75141167-T-C

http://identifiers.org/hco/22/GRCh38#24408268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75141232-C-A

24408441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75141353-G-T

24409241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142182-T-C

24411399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142850-A-G

24411497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142963-T-C

24411497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142963-T-G

24411804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143244-T-C

24411826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143265-A-G

24411826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143265-A-T

http://identifiers.org/hco/22/GRCh38#24412016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75143425-C-A

24412048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143458-G-A

24412048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143458-G-T

http://identifiers.org/hco/22/GRCh38#24412079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75143485-C-A

24412155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143556-T-G

http://identifiers.org/hco/22/GRCh38#24412279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75143612-C-A

24412279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143612-C-G

24412279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143612-C-T

http://identifiers.org/hco/22/GRCh38#24412292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75143625-A-C

24412326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143658-T-G

24412333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143668-G-A

24412333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143668-G-T

http://identifiers.org/hco/22/GRCh38#24412339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75143674-C-A

24412339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143674-C-G

24412467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143768-G-A

24412467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143768-G-C

24412467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75143768-G-T

http://identifiers.org/hco/22/GRCh38#24412741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75143960-C-A

24412741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143960-C-T

http://identifiers.org/hco/22/GRCh38#24413091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75144366-A-C

24413109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144412-C-G

24413181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144477-T-C

http://identifiers.org/hco/22/GRCh38#24413219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75144518-A-C

24413219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144518-A-G

24413488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144775-C-T

24413565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144845-T-C

24413565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144845-T-G

24413744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75145023-T-C

24413974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75145210-A-T

24414005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75145219-A-T

24414640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75145726-C-T

24414682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75145766-A-G

http://identifiers.org/hco/22/GRCh38#24414689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75145773-C-A

24414689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75145773-C-G

http://identifiers.org/hco/22/GRCh38#24414731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75145812-C-A

http://identifiers.org/hco/22/GRCh38#24414806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75145869-A-C

24414806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75145869-A-G

24414806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75145869-A-T

http://identifiers.org/hco/22/GRCh38#24414828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75145889-C-A

24414828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75145889-C-T

http://identifiers.org/hco/22/GRCh38#24414829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75145890-C-A

24414829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75145890-C-T

http://identifiers.org/hco/22/GRCh38#24414866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75145913-C-A

24414866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75145913-C-T

http://identifiers.org/hco/22/GRCh38#24414954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75145989-C-A

24415023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146058-G-A

24415023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146058-G-C

24415023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146058-G-T

24415121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146126-G-A

24415121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146126-G-T

24415185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146186-G-A

24415185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146186-G-T

24415246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146228-G-A

24415246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146228-G-T

24415428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146378-T-C

24415492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146435-G-A

24415492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146435-G-T

http://identifiers.org/hco/22/GRCh38#24415554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75146495-A-C

http://identifiers.org/hco/22/GRCh38#24415622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75146543-C-A

24415622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146543-C-T

24415770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146657-A-G

24415963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75146825-C-T

24416153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147018-G-A

24416192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147073-G-T

24416228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147093-G-T

24416263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147129-G-T

24416692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147459-C-T

24416700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147467-G-A

24416700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147467-G-T

http://identifiers.org/hco/22/GRCh38#24416718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75147472-C-A

24416718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147472-C-G

24416718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147472-C-T

24416760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147519-G-T

24416776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147535-T-A

24416794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147552-G-T

24416804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147571-T-C

24416804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147571-T-G

24416806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147573-G-A

24416806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147573-G-T

24416816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147582-G-A

24416816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147582-G-T

24416826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75147591-T-C

http://identifiers.org/hco/22/GRCh38#24416845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75147609-C-A

http://identifiers.org/hco/22/GRCh38#24416880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75147637-C-A

24417094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148074-G-T

24417184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148160-G-A

24417221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148197-T-G

24417346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148306-G-A

24417346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148306-G-T

24417448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148377-A-G

24417498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148420-C-T

24417552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148484-A-G

24417606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148536-G-A

24417606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148536-G-T

http://identifiers.org/hco/22/GRCh38#24417707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75148625-C-A

24417707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75148625-C-T