53765606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107273403-A-G

53765616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107273393-T-C

http://identifiers.org/hco/1/GRCh38#53765646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107273364-C-A

53765775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107273258-A-G

http://identifiers.org/hco/1/GRCh38#53765804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107273233-C-A

53765811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107273229-A-G

53765835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107273220-G-T

53765970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107273104-G-C

http://identifiers.org/hco/1/GRCh38#53766459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107272697-C-A

53766556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107272631-A-G

http://identifiers.org/hco/1/GRCh38#53766689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107272494-C-A

53766691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107272492-G-T

53766783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107272425-A-G

53766885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107272325-C-T

53767102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107272111-A-G

http://identifiers.org/hco/1/GRCh38#53767240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107271991-C-A

53767254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107271983-G-C

53768695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107270589-T-G

53771256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107269461-G-T

53771739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107268964-G-A

53772087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107268620-T-C

53772297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107268451-G-T

53772300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107268449-T-C

53772368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107268382-G-A

53772450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107268300-T-C

53772482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107268268-T-C

53772513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107268234-C-G

53772542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107268205-G-C

53772825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107267958-T-C

53772921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107267885-T-C

53772953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107267858-G-C

53773073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107267743-G-A

53773312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107267558-T-A

53773396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107267472-A-T

53774563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107266497-T-C

53774692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107266415-C-G

53774753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107266379-G-A

53774753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107266379-G-C

53775103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107266123-C-T

53775296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107265928-A-G

53775363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107265872-T-C

http://identifiers.org/hco/1/GRCh38#53779169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107259885-C-A

53779258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107259811-C-T

53779618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107259534-C-T

53779709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107259444-T-C

53779754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107259398-A-G

53779847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107259310-C-T

53781405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107256689-T-C

53781550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107256546-C-T

53781555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107256537-C-G

53781600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107256490-T-C

53781753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107256364-C-T

http://identifiers.org/hco/1/GRCh38#53781916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#107256208-C-A

53781916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107256208-C-T

http://identifiers.org/hco/1/GRCh38#53782383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107255816-C-A

53782676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107255604-C-T

53783920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107255085-G-A

http://identifiers.org/hco/1/GRCh38#53784258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107254727-C-A

53787010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107253466-T-A

53787010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107253466-T-C

53787013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107253463-T-A

53787013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107253463-T-C

53787025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107253459-G-A

53787025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107253459-G-T

53787035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107253449-T-G

53787234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 107252951-G-T

53787284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107252904-A-G

53787313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107252874-T-A

53789059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107252332-G-T

53789269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107252128-T-C

53789269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107252128-T-G

http://identifiers.org/hco/1/GRCh38#53789294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107252104-C-A

53789294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107252104-C-T

53792205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107251447-G-A

53792213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107251439-A-G

53792329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107251329-T-C

53792437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107251230-T-C

53792437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107251230-T-G

53792596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107251083-G-C

53792614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107251066-A-G

http://identifiers.org/hco/1/GRCh38#53792681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107251004-C-A

53792754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250930-T-G

53792838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250706-T-C

53792927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250626-G-A

53793188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250427-C-G

53793188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250427-C-T

53793334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250286-T-C

53793363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250253-G-A

53793363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250253-G-T

53793384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250234-A-G

http://identifiers.org/hco/1/GRCh38#53793430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107250211-C-A

53793430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107250211-C-T

53795380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107249092-C-T

53795393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107249079-A-G

53795530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248969-A-G

53795595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248916-T-C

53795605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248906-A-G

53795860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248642-G-A

53795919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248580-G-A

53796002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248494-T-A

53796078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248423-T-C

53796082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248419-T-C

53796166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248337-C-T

53796347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107248147-A-G

http://identifiers.org/hco/1/GRCh38#53796518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107248016-C-A

53796622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247935-T-A

53796622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247935-T-C

53796622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247935-T-G

53796632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247925-T-A

53796632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247925-T-C

53796656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247892-G-A

53796656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247892-G-T

53796661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247887-T-C

53796678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247870-T-C

53796868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247685-T-C

53796959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107247596-C-G

53796959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107247596-C-T

http://identifiers.org/hco/1/GRCh38#53797003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107247552-A-C

http://identifiers.org/hco/1/GRCh38#53797104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107247457-A-C

53797196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247366-A-G

53797196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247366-A-T

53797200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247362-G-A

53797200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247362-G-T

53797254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247309-A-G

53797265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247298-T-A

53797265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107247298-T-C

53800625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107246861-T-A

53800815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107246679-C-T

53800902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107246592-T-A

53800902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107246592-T-C

http://identifiers.org/hco/1/GRCh38#53800905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107246589-A-C

53801249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107246315-G-A

53801254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107246310-G-A

53801287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107246290-T-C

53802184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107244672-T-C

53803892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243908-C-G

53803892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243908-C-T

53803939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107243861-A-T

53803987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107243813-A-T

53804020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243780-G-A

53804020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243780-G-T

53804079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243727-T-C

http://identifiers.org/hco/1/GRCh38#53804142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107243708-C-A

53804157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243694-T-C

http://identifiers.org/hco/1/GRCh38#53804325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107243535-A-C

53804799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243389-A-T

53804925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243275-A-G

53804978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107243251-T-C

53805564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107242852-C-T

53805674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107242761-T-G

53806325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107242178-A-G

53806325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107242178-A-T

53806326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107242177-G-T

http://identifiers.org/hco/1/GRCh38#53806338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107242160-A-C

53806338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107242160-A-G

53806366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107242132-A-G

53806448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107242050-T-C

53806483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107242015-T-C

53806524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107241974-A-G

53806524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107241974-A-T

53806534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107241964-A-G

http://identifiers.org/hco/1/GRCh38#53806560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107241899-C-A

53806560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107241899-C-T

53807933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107240691-G-T

53808109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107240555-T-C

53809603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107239004-A-T

53809623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107238984-A-G

53809668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107238940-A-G

http://identifiers.org/hco/1/GRCh38#53809728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107238889-C-A

53809866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107238766-T-C

53810016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107238646-G-A

53810149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107238515-G-C

http://identifiers.org/hco/1/GRCh38#53818733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107238136-A-C

http://identifiers.org/hco/1/GRCh38#53819090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107237784-A-C

53819090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107237784-A-G

53819124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107237763-T-C

53819124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107237763-T-G

53819127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107237760-T-C

53821122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107235807-T-C

53821122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107235807-T-G

53821189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107236088-T-G

53821206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107236072-G-A

53821206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107236072-G-T

53821508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107235774-T-C

53821616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107235674-T-C

53823290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107234110-A-T

http://identifiers.org/hco/1/GRCh38#53823435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107233891-A-C

53823785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107233597-G-T

53823807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107233574-T-A

53824780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107232865-T-A

53825814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107232395-G-T

http://identifiers.org/hco/1/GRCh38#53826104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107232113-C-A

53826271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231962-A-G

53827703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231816-C-T

53827725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231798-T-A

http://identifiers.org/hco/1/GRCh38#53827888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107231628-C-A

53827888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231628-C-T

53827951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231568-G-T

53827958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231561-A-G

53827958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231561-A-T

53828016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107231499-G-A

53828129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107231386-T-C

53828240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231282-T-A

53828240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231282-T-C

53828651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230891-G-T

53828692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230862-A-G

53828730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230824-G-A

53828755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230800-G-T

http://identifiers.org/hco/1/GRCh38#53828758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107230797-C-A

53828758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230797-C-G

53828773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230781-G-A

53829362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230152-T-C

53831974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107229139-T-C

53832284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228876-A-G

http://identifiers.org/hco/1/GRCh38#53832337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107228828-A-C

http://identifiers.org/hco/1/GRCh38#53832651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107228397-C-A

53833059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228046-T-C

53835252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226241-T-A

53835275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226218-T-A

53835278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226215-G-A

53835278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226215-G-T

53835288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226206-T-A

53835288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226206-T-C

53835371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226138-C-T

53835528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107226044-A-G

53835649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107225925-A-G

53837813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107225702-C-T

http://identifiers.org/hco/1/GRCh38#53838131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#107225393-C-A

53838131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107225393-C-T

http://identifiers.org/hco/1/GRCh38#53838146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107225378-A-C

53838146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107225378-A-G

53838185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107225360-A-G

53838185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107225360-A-T

53838246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107225299-T-A

53838246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107225299-T-C

53838276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107225269-C-G

53838302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 107225243-G-A

53838302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 107225243-G-C

53838302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 107225243-G-T

53838416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non coding transcript exon variant
orthologous variants: 107225129-G-A

53838416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non coding transcript exon variant
orthologous variants: 107225129-G-C

53838416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25525
most severe consequence: non coding transcript exon variant
orthologous variants: 107225129-G-T