49791178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99319952-A-G

49791178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99319952-A-T

49791191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99319965-A-G

http://identifiers.org/hco/12/GRCh38#49791278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99320032-C-A

49791278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320032-C-T

49791290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320051-A-G

49791290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320051-A-T

http://identifiers.org/hco/12/GRCh38#49791327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99320085-C-A

49791327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320085-C-G

49791327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320085-C-T

49791381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320139-A-G

49791395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320151-G-A

49791395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320151-G-T

49791465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320221-G-A

49791465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320221-G-T

49791530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320286-T-A

49791530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320286-T-C

49791566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320314-T-A

49791566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320314-T-C

49791566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320314-T-G

49791617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320364-A-G

49791661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320408-C-T

http://identifiers.org/hco/12/GRCh38#49791710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99320449-C-A

http://identifiers.org/hco/12/GRCh38#49791725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99320463-C-A

http://identifiers.org/hco/12/GRCh38#49791775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99320515-A-C

49791792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320534-A-G

http://identifiers.org/hco/12/GRCh38#49791832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99320573-C-A

49791832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320573-C-G

49791832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3 prime UTR variant
orthologous variants: 99320573-C-T

49791998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 99320739-C-T

http://identifiers.org/hco/12/GRCh38#49792011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99320749-C-A

49792011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 99320749-C-G

49792011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 99320749-C-T

http://identifiers.org/hco/12/GRCh38#49792035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99320773-C-A

49792035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 99320773-C-T

49792326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99320916-A-G

http://identifiers.org/hco/12/GRCh38#49792500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99321071-C-A

49792500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99321071-C-T

49792561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99321132-G-T

http://identifiers.org/hco/12/GRCh38#49792624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99321195-C-A

49792684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99321253-G-A

49792784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99321353-T-C

49792845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99321414-G-A

49792845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99321414-G-T

http://identifiers.org/hco/12/GRCh38#49792874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99321443-C-A

49792874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99321443-C-T

49792898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99321467-A-G

49793034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99321589-G-T

49793154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99321684-G-T

http://identifiers.org/hco/12/GRCh38#49793211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99321723-A-C

49793211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99321723-A-G

http://identifiers.org/hco/12/GRCh38#49793226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99321747-C-A

49793267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99321790-G-A

49793267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99321790-G-C

49793267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99321790-G-T

49793287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99321808-T-C

49793356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99321838-G-T

49793364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99321846-A-G

49793380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99321862-G-A

49793380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99321862-G-T

49793395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99321877-C-T

49793437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 99321919-T-G

49793481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99321976-A-T

49793752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99322014-G-A

49793752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: stop gained
orthologous variants: 99322014-G-T

http://identifiers.org/hco/12/GRCh38#49793860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99322122-C-A

49793860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99322122-C-T

49793953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322715-G-A

49793953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322715-G-T

http://identifiers.org/hco/12/GRCh38#49794006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99322768-C-A

49794006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322768-C-G

49794006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322768-C-T

49794014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322776-A-G

http://identifiers.org/hco/12/GRCh38#49794034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99322788-A-C

49794039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322793-T-C

http://identifiers.org/hco/12/GRCh38#49794045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99322802-C-A

49794045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322802-C-T

http://identifiers.org/hco/12/GRCh38#49794046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99322803-A-C

49794046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322803-A-T

49794116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322871-T-C

49794117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322872-G-A

49794211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322937-T-C

49794220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99322946-C-T

49794336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99323061-A-G

49794622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99323354-T-A

49794622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99323354-T-C

49794622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99323354-T-G

49794679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99323387-G-A

49794679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99323387-G-T

http://identifiers.org/hco/12/GRCh38#49794682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99323390-C-A

49794682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99323390-C-T

http://identifiers.org/hco/12/GRCh38#49794747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99323417-C-A

49794747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99323417-C-T

http://identifiers.org/hco/12/GRCh38#49794814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99323483-C-A

49794814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99323483-C-G

49794814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99323483-C-T

49794845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99323514-G-A

49794845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99323514-G-T

49794861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99323530-G-A

49794861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99323530-G-T

49794866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99323535-A-G

49794911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99323577-T-C

49795021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99323687-C-G

49795073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99323739-T-C

49795238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99323904-A-G

http://identifiers.org/hco/12/GRCh38#49795243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99323909-C-A

49795243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99323909-C-G

49795243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99323909-C-T

49795343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99324009-G-A

49795343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99324009-G-T

http://identifiers.org/hco/12/GRCh38#49795374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99324040-C-A

49795374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99324040-C-T

http://identifiers.org/hco/12/GRCh38#49795385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99324051-C-A

49795385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99324051-C-T

49795705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99324365-G-C

http://identifiers.org/hco/12/GRCh38#49796015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#99324672-A-C

49796015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99324672-A-G

49796033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99324690-G-A

49796075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99324729-A-G

49796129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99324783-G-T

49796416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325070-G-A

49796416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325070-G-C

49796416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99325070-G-T

http://identifiers.org/hco/12/GRCh38#49796457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99325111-C-A

49796457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325111-C-T

49796606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99325260-G-A

49796606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99325260-G-T

49796888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99325542-T-C

49796995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325649-C-G

49796995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325649-C-T

49796999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325653-G-C

49796999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325653-G-T

http://identifiers.org/hco/12/GRCh38#49797000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99325654-C-A

49797000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325654-C-T

49797016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: stop gained
orthologous variants: 99325670-G-A

49797016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325670-G-C

49797016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325670-G-T

49797018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325672-G-A

49797018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99325672-G-T

http://identifiers.org/hco/12/GRCh38#49797137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99325791-C-A

49797137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99325791-C-T

49797242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99325896-G-A

49797263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99325917-C-T

49797402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 99326056-G-A

49797402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 99326056-G-T

49797441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99326095-G-A

49797441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99326095-G-T

49797640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99326340-T-C

49797786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99326643-G-C

49797834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99326691-G-C

49797836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99326693-C-T

http://identifiers.org/hco/12/GRCh38#49797850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99326707-C-A

49797892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, undefined
orthologous variants: 99326743-G-C

49798018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99326862-T-A

49798018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99326862-T-C

49798200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327039-G-A

http://identifiers.org/hco/12/GRCh38#49798209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99327071-A-C

49798209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327071-A-G

49798237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327099-G-A

49798237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327099-G-T

http://identifiers.org/hco/12/GRCh38#49798252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99327125-A-C

49798252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327125-A-G

49798260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327133-C-T

49798270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327143-A-G

http://identifiers.org/hco/12/GRCh38#49798324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99327194-C-A

49798324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327194-C-T

http://identifiers.org/hco/12/GRCh38#49798415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99327300-A-C

49798415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99327300-A-G

49798415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense variant
orthologous variants: 99327300-A-T

49798440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99327325-T-C

49798449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: synonymous variant
orthologous variants: 99327334-T-G

49798515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327372-T-C

http://identifiers.org/hco/12/GRCh38#49798592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99327436-C-A

49798592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327436-C-G

49798592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327436-C-T

http://identifiers.org/hco/12/GRCh38#49798711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99327563-A-C

49798726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327578-A-G

49798798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99327635-C-T

49799234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99328278-C-G

49800729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99329424-G-A

49801366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99329904-C-T

http://identifiers.org/hco/12/GRCh38#49801488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99330059-C-A

http://identifiers.org/hco/12/GRCh38#49802545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99330882-C-A

49802545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330882-C-T

http://identifiers.org/hco/12/GRCh38#49802546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99330883-C-A

49802546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330883-C-T

http://identifiers.org/hco/12/GRCh38#49802584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99330920-A-C

49802584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330920-A-G

49802596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330932-G-A

49802596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330932-G-T

http://identifiers.org/hco/12/GRCh38#49802608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99330944-A-C

49802608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330944-A-G

49802608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330944-A-T

http://identifiers.org/hco/12/GRCh38#49802622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99330958-C-A

49802622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330958-C-T

http://identifiers.org/hco/12/GRCh38#49802624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99330960-A-C

49802624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330960-A-G

49802624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330960-A-T

http://identifiers.org/hco/12/GRCh38#49802667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99330991-C-A

49802667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330991-C-G

49802667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99330991-C-T

49802704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99331028-T-C

49802826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99331142-T-A

49802826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99331142-T-C

49802946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99331313-T-C

49803168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99331522-G-A

49803168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99331522-G-T

49803208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99331542-G-A

49803852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99331866-A-G

http://identifiers.org/hco/12/GRCh38#49803864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99331876-C-A

49803864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99331876-C-T

49803872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99331884-C-T

http://identifiers.org/hco/12/GRCh38#49803876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99331888-A-C

49803889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99331895-G-A

49803889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99331895-G-T

http://identifiers.org/hco/12/GRCh38#49803909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99331915-C-A

49803909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99331915-C-T

49803917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99331916-C-T

http://identifiers.org/hco/12/GRCh38#49803938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99331937-C-A

49803938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99331937-C-T

49803943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99331942-C-T

http://identifiers.org/hco/12/GRCh38#49803992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99331991-C-A

49803992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99331991-C-T

49804034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99332033-G-A

49804034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99332033-G-T

49804097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332086-G-A

49804097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332086-G-C

49804097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332086-G-T

49804103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332100-A-G

49804170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332150-A-G

http://identifiers.org/hco/12/GRCh38#49804173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99332153-C-A

49804173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332153-C-T

49804181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332161-T-G

49804313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332283-C-G

http://identifiers.org/hco/12/GRCh38#49804317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99332287-A-C

49804317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332287-A-G

49804357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332306-T-C

http://identifiers.org/hco/12/GRCh38#49804422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99332371-A-C

49804989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332713-G-A

49804989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332713-G-C

http://identifiers.org/hco/12/GRCh38#49805046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99332778-C-A

49805046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332778-C-T

49805116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332840-G-A

http://identifiers.org/hco/12/GRCh38#49805118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99332842-C-A

49805118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332842-C-G

http://identifiers.org/hco/12/GRCh38#49805153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99332874-C-A

49805153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332874-C-T

http://identifiers.org/hco/12/GRCh38#49805155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99332876-C-A

49805155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332876-C-T

http://identifiers.org/hco/12/GRCh38#49805190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99332928-C-A

49805190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332928-C-T

49805200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99332966-C-G

http://identifiers.org/hco/12/GRCh38#49805309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99333075-C-A

http://identifiers.org/hco/12/GRCh38#49805352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99333122-C-A

49805352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99333122-C-T

49805418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99333185-A-G

http://identifiers.org/hco/12/GRCh38#49805435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99333213-C-A

49805435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99333213-C-G

49805934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99333845-G-A

49805934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron variant
orthologous variants: 99333845-G-T

http://identifiers.org/hco/12/GRCh38#49805945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99333874-C-A

49805945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99333874-C-T

49805987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99333916-T-C

49806005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99333932-G-T

http://identifiers.org/hco/12/GRCh38#49806017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99333944-C-A

http://identifiers.org/hco/12/GRCh38#49806072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99333996-C-A

49806072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99333996-C-T

http://identifiers.org/hco/12/GRCh38#49806140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99334043-C-A

49806140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99334043-C-T

49806145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99334048-A-G

http://identifiers.org/hco/12/GRCh38#49806660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99334550-A-C

49806718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99334618-C-G

49806758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99334685-C-T

49806863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99334790-T-C

49806953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99334845-C-T

49807078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99334941-A-G

49807420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99335438-C-G

49807601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99335724-C-T

49808064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99336227-T-C

http://identifiers.org/hco/12/GRCh38#49808189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99336381-A-C

49808189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99336381-A-T

http://identifiers.org/hco/12/GRCh38#49808422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99336710-C-A

49808439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99336734-C-G

49808466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99336762-G-A

49808466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99336762-G-T

49808558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99336891-A-G

49808591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99336924-T-G

49808616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99336947-C-T

49808714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99337012-C-T

49809259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338331-G-T

49809543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338587-C-T

49809644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338664-A-G

49809716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338734-G-A

49809832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338815-C-G

49810048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99339007-G-T

49810406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99339318-G-A

49810460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99339370-G-T

49821254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99347241-T-C

49821418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99347412-A-G

49821467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99347459-G-A

49821485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99347475-C-T

49821583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99347568-G-A

49821583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99347568-G-C

49821803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99347851-G-A

49821842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99347891-C-T

49822026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99348043-G-A

49823082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99349721-T-C

49823155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99349792-C-G

49823258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99350255-C-G

49823289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99350286-G-A

49823857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99350821-G-A

49823973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99350935-G-A

49824310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351229-C-T

49824327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351246-A-G

49824424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351479-A-T

49824439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351494-T-A

49824439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351494-T-C

49824484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351599-G-T

49824674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351755-T-C

49824841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351879-T-C

49824880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351890-A-G

49825207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99352567-C-G

http://identifiers.org/hco/12/GRCh38#49825239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99352599-C-A

49825401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99352786-A-G

49825401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99352786-A-T

http://identifiers.org/hco/12/GRCh38#49825544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99352920-A-C

http://identifiers.org/hco/12/GRCh38#49825768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99353145-A-C

49825768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99353145-A-G

49825923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99353274-G-A

http://identifiers.org/hco/12/GRCh38#49826394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99353664-A-C

49826705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99353992-G-A

49826877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99354135-G-A

49826879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99354137-C-T

49826896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99354151-G-A

49827075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99354290-A-G

49827324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99354549-C-T

http://identifiers.org/hco/12/GRCh38#49827814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99355018-C-A

49827814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355018-C-T

49827881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99355084-T-C

49828013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99355211-C-T

49828177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355372-T-C

49828177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355372-T-G

49828194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355392-G-A

49828194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355392-G-T

49828394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355591-G-A

49828394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355591-G-T

49828420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355617-G-A

49828420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355617-G-T

http://identifiers.org/hco/12/GRCh38#49828470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99355667-C-A

http://identifiers.org/hco/12/GRCh38#49828473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99355670-A-C

http://identifiers.org/hco/12/GRCh38#49828539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99355736-C-A

49828539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99355736-C-T

49828554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355751-G-A

49828554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355751-G-T

http://identifiers.org/hco/12/GRCh38#49828566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99355763-A-C

49828566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99355763-A-G

49828600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355797-G-A

49828600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355797-G-T

49828648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355853-G-A

49828648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355853-G-C

49828650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355855-G-A

49828650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355855-G-T

49828671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355876-C-T

http://identifiers.org/hco/12/GRCh38#49828706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99355929-C-A

49828706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99355929-C-T