http://identifiers.org/hco/22/GRCh38#48489616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87428716-C-A

48489616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: synonymous variant
orthologous variants: 87428716-C-T

http://identifiers.org/hco/22/GRCh38#48489747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87428845-C-A

48489747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87428845-C-G

48489747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87428845-C-T

http://identifiers.org/hco/22/GRCh38#48489759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87428860-C-A

48489759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87428860-C-T

48489928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429011-G-A

48489928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429011-G-C

http://identifiers.org/hco/22/GRCh38#48490071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87429132-C-A

48490268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429310-A-G

48490388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429424-C-G

48490475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429484-C-T

48490727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429725-A-G

48490832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429843-T-A

48490864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429875-G-A

http://identifiers.org/hco/22/GRCh38#48490922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87429915-A-C

48490922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87429915-A-T

48491030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87430039-G-A

48491176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87430130-G-T

48491180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87430134-G-A

http://identifiers.org/hco/22/GRCh38#48491355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87430307-C-A

48491652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87430593-C-T

48492131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87430984-C-T

48492907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87431708-C-T

48493078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87431832-G-A

http://identifiers.org/hco/22/GRCh38#48493115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87431855-C-A

48493953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87432683-C-T

48493985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87432723-C-T

48494054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87432816-T-C

48494089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87432845-C-G

48494193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87432926-C-T

http://identifiers.org/hco/22/GRCh38#48495159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87433789-C-A

48495159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87433789-C-T

48495249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87433845-G-C

48496770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87434216-G-A

48496829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87434266-C-T

48496830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87434267-G-A

48496868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87434303-T-C

48498229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87435132-G-T

48498856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87435713-C-T

http://identifiers.org/hco/22/GRCh38#48498950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87435804-C-A

48499078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87435915-G-A

48499222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87436070-C-T

http://identifiers.org/hco/22/GRCh38#48499447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87436304-C-A

48500205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87437680-G-A

48500250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87437726-T-C

48500358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87437840-G-A

48500509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87437964-G-A

48500565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438004-G-A

48500565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438004-G-C

48500772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438144-C-G

48500786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438160-T-C

48500814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438173-T-A

48501089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438447-C-T

48501168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438518-C-T

48501454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438818-G-A

48501454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438818-G-C

48501510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87438896-A-G

48501683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87439070-T-C

48501886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87439280-G-A

48502079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87439457-C-G

48502367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87439732-C-T

48502916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87439983-A-G

48513668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87446826-G-A

48513894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447035-C-T

48514179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447387-G-A

48514179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447387-G-C

48514190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447398-A-G

48514228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447436-C-T

48514369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447581-T-A

48514442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447653-C-G

48514501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447721-G-A

48514501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447721-G-T

48514551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447790-A-G

48514727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87447843-C-T

48514906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448029-C-G

http://identifiers.org/hco/22/GRCh38#48515403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87448366-C-A

48515424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448372-C-G

48515531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448472-G-A

48515557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448506-C-T

48515575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448530-G-A

48515591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448550-A-G

48515593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448552-C-T

48515624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448595-G-A

48515723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448691-G-A

48515723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448691-G-C

48515917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448858-G-A

48515917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448858-G-C

48515917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87448858-G-T

http://identifiers.org/hco/22/GRCh38#48515984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87448928-C-A

48516068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87449013-T-C

48516466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87449399-C-G

48516466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87449399-C-T

48516907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87449757-G-A

48516918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87449768-C-T

48516960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87449799-G-A

48517059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87449902-C-T

48517168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87449986-G-T

48517228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87450045-C-T

48517231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87450048-C-G

48517231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87450048-C-T

48517599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87450573-G-A

48517601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87450575-G-T

48517643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87450653-G-A

48517993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87451033-G-A

48517999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87451039-G-A

48518117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87451128-G-T

48518172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87451179-G-A

48518172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87451179-G-C

48518464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87451380-G-A

48518724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87451632-C-G

48518931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87451818-G-A

48519441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87452262-G-A

48520878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87453111-G-A

48520897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87453137-T-G

48520902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87453140-G-T

48521283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87453447-G-C

48521284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87453448-G-A

48521385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87453547-A-G

48521425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, undefined
orthologous variants: 87453587-T-C

48521442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87453603-A-G

48523376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454049-C-T

48523403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454074-G-A

48523410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454081-C-T

48523411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454082-G-A

48523525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454191-G-A

http://identifiers.org/hco/22/GRCh38#48523970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87454536-A-C

48523970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454536-A-G

48524141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454683-G-A

48524356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454885-G-A

48524357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87454886-A-G

48526237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87459663-T-A

48527057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87460401-A-G

http://identifiers.org/hco/22/GRCh38#48527097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87460440-C-A

http://identifiers.org/hco/22/GRCh38#48530113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87464096-C-A

48530113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464096-C-G

48530255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464232-G-A

48530382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464375-A-T

48530468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464464-G-A

48530526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464519-G-A

http://identifiers.org/hco/22/GRCh38#48530572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87464558-C-A

48530572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464558-C-T

48530678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464668-A-T

http://identifiers.org/hco/22/GRCh38#48530789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87464781-C-A

48530868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464861-C-T

48530871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464864-C-T

48530945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464942-G-A

48530972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464978-G-A

48530972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87464978-G-C

48531022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87465028-C-G

48531037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87465043-G-A

48531048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87465054-C-T

48532061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87466353-C-T

48532083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87466370-C-T

48535414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87467314-A-G

48535538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87467443-C-T

48536243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87468236-G-A

48537176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87469086-C-T

48538562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87470591-T-C

48538677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87470718-A-G

48538677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87470718-A-T

48538697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87470737-T-G

48538719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87470767-A-T

48539186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87471507-T-A

48539186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87471507-T-C

48539337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87471656-C-T

48539411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87471728-C-G

48539427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87471743-G-A

48539603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87471931-G-A

48539824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87472163-C-G

48540354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87472817-G-A

48540355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87472818-G-C

48540422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87472888-C-T

48540450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87472916-G-A

http://identifiers.org/hco/22/GRCh38#48540501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87472953-C-A

48540532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87472984-C-T

48540583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87473026-C-T

48540656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87473088-T-G

48540684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87473119-G-A

48540684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87473119-G-T

48543044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87474056-T-G

48543105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87474117-C-T

48543175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87474189-T-G

http://identifiers.org/hco/22/GRCh38#48543184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87474200-C-A

48543184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87474200-C-T

48543243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87474262-C-T

48543251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87474270-C-T

48543282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87474301-T-C

http://identifiers.org/hco/22/GRCh38#48543294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87474313-C-A

48543367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474386-G-A

48543367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474386-G-T

48543449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474465-A-G

48543449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474465-A-T

48543560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474565-A-G

48543560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474565-A-T

48543562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474567-G-A

48543562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474567-G-T

48543580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474579-T-C

48543588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474588-G-A

48543588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474588-G-C

48543591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474591-G-T

48543964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474895-G-A

48543984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474909-G-T

48543997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474922-A-G

48544041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474947-T-G

48544074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474989-G-A

48544074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474989-G-T

48544079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474994-G-A

48544079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87474994-G-T

48544114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475022-A-G

48544128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475034-G-A

48544128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475034-G-T

48544134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475040-G-A

48544134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475040-G-T

48544164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475066-T-G

48544222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475095-A-G

http://identifiers.org/hco/22/GRCh38#48544357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475183-C-A

48544357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475183-C-G

48544357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475183-C-T

http://identifiers.org/hco/22/GRCh38#48544365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475189-C-A

48544365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475189-C-G

48544410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475236-C-G

48544445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475270-C-T

48544458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475283-G-A

48544458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475283-G-T

http://identifiers.org/hco/22/GRCh38#48544465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475290-C-A

48544672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87475506-T-C

48544708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475544-G-A

48544719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475555-G-T

48544779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475616-C-G

http://identifiers.org/hco/22/GRCh38#48544908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475704-A-C

48544908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475704-A-T

http://identifiers.org/hco/22/GRCh38#48544925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475725-C-A

48544925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87475725-C-T

48544946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475749-T-A

http://identifiers.org/hco/22/GRCh38#48545038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475843-C-A

48545038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475843-C-T

48545044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475849-G-T

48545097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475894-T-A

48545107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475904-C-T

http://identifiers.org/hco/22/GRCh38#48545138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475926-A-C

http://identifiers.org/hco/22/GRCh38#48545139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475927-C-A

48545139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475927-C-T

http://identifiers.org/hco/22/GRCh38#48545186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87475975-C-A

48545186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475975-C-G

48545186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87475975-C-T

48545249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87476028-G-A

48545249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87476028-G-C

48545249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87476028-G-T

48545362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87476146-A-G

48545362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87476146-A-T

48545722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476645-G-T

48545723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476646-A-G

http://identifiers.org/hco/22/GRCh38#48545748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87476671-C-A

48545793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476727-G-T

48545808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476742-G-A

48545808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476742-G-T

48545833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476767-G-A

48545833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476767-G-C

48545934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476892-C-G

48545934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476892-C-T

48545943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87476901-G-A

http://identifiers.org/hco/22/GRCh38#48546427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87477333-C-A

48546427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477333-C-T

http://identifiers.org/hco/22/GRCh38#48546433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87477340-C-A

48546435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477342-G-A

48546435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477342-G-T

48546448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477355-G-A

48546490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477389-G-A

48546490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477389-G-T

48546492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477391-G-A

48546549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477435-C-T

http://identifiers.org/hco/22/GRCh38#48546590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87477468-A-C

48546634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477495-G-A

48546643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477504-G-A

48546643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477504-G-C

48546748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477577-G-T

48546758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477587-G-A

48546758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477587-G-T

48546761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477590-T-G

48546765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477594-T-G

48546766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477595-A-G

48546778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477611-G-C

48546778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477611-G-T

48546788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477614-G-C

48546788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477614-G-T

48546824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477653-A-G

48546912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87477739-T-C

48547066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477897-C-G

48547083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477914-G-A

48547083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477914-G-C

48547083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87477914-G-T

48547283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87478141-G-A

48547283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87478141-G-T

48547321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87478184-A-G

48547385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87478253-T-C

http://identifiers.org/hco/22/GRCh38#48547515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87478353-C-A

48547515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87478353-C-T

48548831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87480385-T-C

http://identifiers.org/hco/22/GRCh38#48548856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87480409-A-C

http://identifiers.org/hco/22/GRCh38#48549085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87480614-C-A

48549169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87480697-T-C

48549208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87480733-C-T

48549351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87480874-A-G

48549639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87481129-A-G

48549845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87481320-G-T

48550546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483513-A-G

http://identifiers.org/hco/22/GRCh38#48550566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87483529-C-A

48550613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483564-C-T

48550653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483585-T-C

48550720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483655-G-T

48550755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483685-G-A

48550766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483696-G-A

48550819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483736-G-T

48550869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483810-C-T

48550879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483820-T-G

48551076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483951-C-T

48551077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87483952-G-A

48551146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484018-T-A

48551395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484237-G-A

48551644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484404-C-T

48551645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484405-A-T

48551855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484571-C-T

48552009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484703-C-T

48552061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484747-G-A

48552087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484773-T-C

48552174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484846-C-T

48552214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484884-A-G

48552288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484927-A-G

48552347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87484974-G-A

http://identifiers.org/hco/22/GRCh38#48552421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87485058-C-A

48552463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87485083-C-T

48552464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87485084-G-A

48552606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87485234-G-A

48552655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87485283-G-A

48553747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87486923-C-T

48553966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87487152-G-A

http://identifiers.org/hco/22/GRCh38#48554061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87487231-C-A

48554384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87487525-T-A

48554384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87487525-T-C

48554846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87487983-G-A

48554917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87488047-G-T

48555318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87488785-T-A

48555397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87488883-G-C

48555419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87488906-G-A

48555419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87488906-G-C

48555536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87489011-T-C

48555700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87489127-C-T

48556078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87489441-G-A

48556162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87489519-C-G

48556584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87489948-G-T

48556586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87489950-C-T

48556769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87490096-T-C

48556772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87490099-G-C

48557375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87492164-G-A

http://identifiers.org/hco/22/GRCh38#48557399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87492183-C-A

48557407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87492191-T-C

48557436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87492220-C-T

48558018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87492535-G-C

48558076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87492585-T-C

48558431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87492937-G-A

48561119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494002-G-A

48561119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494002-G-C

48561189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494072-G-A

48561229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494117-A-T

48561287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494204-C-T

http://identifiers.org/hco/22/GRCh38#48561336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87494262-C-A

48561387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494320-G-A

48561390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494323-C-G

48561390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494323-C-T

48561466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494365-C-G

48561466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494365-C-T

48561468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494367-T-C

48561690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494591-T-C

48561823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87494723-G-A

48562920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87495347-G-A

48562929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87495356-G-A

48563092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87495481-C-T

48563108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87495497-A-G

48563111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87495500-A-G

48563121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87495509-G-A

48563147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87495530-A-G

48563157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87495540-G-A

http://identifiers.org/hco/22/GRCh38#48563162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87495545-C-A

48565404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87496288-T-C

48565460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87496347-T-C

48566074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87497255-A-G

48566149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87497333-G-A

48566294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87497523-A-G

48566400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87497653-A-G

http://identifiers.org/hco/22/GRCh38#48566574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87497889-A-C

48566777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87498200-C-G

48566898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87498298-C-T

http://identifiers.org/hco/22/GRCh38#48566905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87498305-C-A

48566907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87498307-G-A

48567259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87498959-G-A

48567759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87499367-G-A

48567991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87499530-C-G

48568516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87499997-G-A

48568516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87499997-G-C

48568552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87500033-C-T

48572506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87505896-G-A

48572794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87506176-G-A

48572798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87506180-C-T

48573077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87506453-G-A

48573229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87506596-G-A

48573385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87506724-T-G

48573784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507074-G-A

48573885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507128-G-T

48573887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507130-C-T

48573918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507157-C-T

48574082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507320-G-C

48574292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507505-G-T

48574325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507539-C-T

48574485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507677-G-A

48574750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87507880-G-A

http://identifiers.org/hco/22/GRCh38#48575291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87508404-A-C

48576629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87509734-T-A

48576629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87509734-T-C

48576629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87509734-T-G

48576752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87509844-G-T

48577103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87510222-G-T

48577109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87510228-G-C

48577610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87510653-T-C

48577625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87510666-G-A

48577630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87510671-C-G

48577699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87510718-G-A

48577710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87510728-G-A

48577790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87510790-G-C

48577791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87510791-G-C

48577970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87510961-T-C

48578201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511263-G-C

48578314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511336-T-A

48578379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511375-C-G

48578472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511471-G-A

48578670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511702-A-G

48578670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511702-A-T

48578686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511721-T-C

48578743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511784-T-C

48578834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511884-G-A

48578864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511924-G-C

48578864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511924-G-T

48578866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87511926-G-A

48579224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87512259-G-A

48579372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87512396-C-T

48579561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87512550-C-G

48579778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87512711-G-A

48579821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87512758-G-A

http://identifiers.org/hco/22/GRCh38#48580164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87513107-A-C

48580241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87513186-G-A

48580283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87513228-G-A

48580589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514509-G-A

48580633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514549-G-A

48580633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514549-G-T

48580661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514576-G-A

http://identifiers.org/hco/22/GRCh38#48580730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87514618-C-A

48580832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514681-C-T

48580902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514726-A-G

48580902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514726-A-T

48580926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514750-G-A

48580926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514750-G-T

http://identifiers.org/hco/22/GRCh38#48581138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87514942-C-A

48581138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87514942-C-T

48581237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87515034-C-G

48581425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87515217-C-T

http://identifiers.org/hco/22/GRCh38#48581795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87515506-A-C

48582027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87515715-G-A

48582154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87515841-C-T

48582388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516070-T-C

48582429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516104-C-T

48582464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516139-T-A

48582464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516139-T-C

48582489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516158-C-T

48582523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516190-C-G

http://identifiers.org/hco/22/GRCh38#48582533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516200-A-C

48582534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516201-A-G

48582535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516202-T-A

48582535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516202-T-C

48582608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516273-C-G

48582614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516279-A-G

48582614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516279-A-T

48582668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516336-T-A

48582668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516336-T-C

48582684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516349-T-A

48582684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516349-T-C

http://identifiers.org/hco/22/GRCh38#48582686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516351-C-A

48582686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516351-C-T

48582753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516446-C-T

http://identifiers.org/hco/22/GRCh38#48582774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516464-C-A

48582774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516464-C-T

48582817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516514-C-T

48582850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516550-A-G

http://identifiers.org/hco/22/GRCh38#48582857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516558-A-C

48582857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516558-A-G

http://identifiers.org/hco/22/GRCh38#48582878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516571-A-C

http://identifiers.org/hco/22/GRCh38#48582980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516662-A-C

48582980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516662-A-G

http://identifiers.org/hco/22/GRCh38#48583009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516693-A-C

48583009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516693-A-G

48583018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516702-C-T

48583049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516733-G-A

48583049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516733-G-C

48583049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516733-G-T

http://identifiers.org/hco/22/GRCh38#48583136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516807-C-A

http://identifiers.org/hco/22/GRCh38#48583148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87516814-C-A

48583148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516814-C-G

48583148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516814-C-T

48583170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516828-C-G

48583194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516842-A-G

48583208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516856-T-A

48583208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87516856-T-C

48587580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521070-T-C

48587600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521095-G-A

48587658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521154-G-A

48587687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521171-C-T

48587717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521199-C-T

48587718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521200-C-T

48587772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521229-C-T

48587861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521297-G-T

48587884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521319-G-A

48587891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521326-G-A

48587936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521385-T-C

48588028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521449-T-A

48588060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521478-T-C

48588143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521557-T-C

48588191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521609-G-A

48588360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521790-C-T

48588407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521848-G-A

48588462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521894-C-G

48588462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521894-C-T

48588477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521907-C-T

48588570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521990-C-G

48588570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87521990-C-T

http://identifiers.org/hco/22/GRCh38#48588732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87522132-A-C

48588752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522365-G-A

48588811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522423-C-T

48588815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522427-G-A

48588840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522444-G-A

http://identifiers.org/hco/22/GRCh38#48588846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87522450-A-C

48588846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522450-A-G

48588851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522455-G-A

48588863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522466-C-T

48588944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522530-G-A

48589000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522584-G-A

48589342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522908-T-C

48589347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87522912-A-G

48590029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87523965-C-T

48590103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524068-G-A

http://identifiers.org/hco/22/GRCh38#48590161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87524121-C-A

48590161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524121-C-G

48590161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524121-C-T

48590167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524127-G-A

48590180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524140-G-A

48590228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524187-C-T

48590264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524222-T-C

48590564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524513-C-T

48590566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87524514-G-C

48593253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87526574-T-C

48593274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87526598-G-T

48593327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87526648-G-A

48593327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87526648-G-C

48593646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87526919-C-T

48593657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87526930-C-T

48595113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87528651-C-G

48595113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87528651-C-T

48595276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87528809-T-C

48595277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87528810-C-G

48595339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87528846-G-A

48595393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87528895-G-A

48595645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87529159-G-A

48596297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87529791-C-T

48596366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87529846-C-G

48596366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87529846-C-T

http://identifiers.org/hco/22/GRCh38#48596373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87529853-C-A

48597613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87530170-C-T

48597761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87530299-G-A

48597819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87530352-G-T

48597947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87530518-C-T

48598404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87530922-G-A

48598587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531105-C-T

48598660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531171-T-C

48598843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531292-G-A

48598862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531311-T-G

48598886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531335-C-T

48598925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531354-A-G

http://identifiers.org/hco/22/GRCh38#48599163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87531555-C-A

48599191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531583-C-T

http://identifiers.org/hco/22/GRCh38#48599223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87531611-A-C

48599223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531611-A-G

48599291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531678-G-C

48599445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531809-A-T

48599609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531969-G-A

48599609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531969-G-C

48599609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87531969-G-T

48599655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532014-G-A

48599668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532026-G-C

48599697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532044-G-A

48599710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532058-G-A

48599710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532058-G-C

48599710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532058-G-T

48599728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532076-T-C

http://identifiers.org/hco/22/GRCh38#48599798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87532171-C-A

48599798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532171-C-T

48599811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532184-G-A

48599819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532195-T-A

48599819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532195-T-C

48599880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532287-C-T

48600047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87532474-C-T

http://identifiers.org/hco/22/GRCh38#48600168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87532601-C-A

http://identifiers.org/hco/22/GRCh38#48600182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87532615-A-C

http://identifiers.org/hco/22/GRCh38#48604347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87533792-C-A

48604347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87533792-C-T

48604358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87533802-C-T

48604435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87533875-G-C

http://identifiers.org/hco/22/GRCh38#48604467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87533901-A-C

48604603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534030-C-T

48604829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534236-A-G

48605006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534522-C-T

48605219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534762-G-A

48605219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534762-G-T

48605321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534861-G-A

48605321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534861-G-T

48605371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534917-G-A

48605384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534933-A-G

48605398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534947-A-G

48605409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534958-T-G

48605441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534990-G-A

48605447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87534996-A-T

48605451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535000-C-G

48605451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535000-C-T

48605452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535001-A-G

48605456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535005-G-A

48605524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535074-G-C

48605615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535140-C-G

48605668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535192-C-T

48605739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535251-C-G

48605739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535251-C-T

48605795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535278-G-T

48605800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535283-C-T

http://identifiers.org/hco/22/GRCh38#48605847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87535307-C-A

48606149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535624-C-T

48606216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535700-G-C

48606295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87535769-G-A

48606558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87536037-G-T

48606572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87536054-C-T

http://identifiers.org/hco/22/GRCh38#48606665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87536147-C-A

48606665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87536147-C-T

48606712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87536189-A-T

48608008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87536642-G-A

48608008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87536642-G-T

http://identifiers.org/hco/22/GRCh38#48608266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87536874-A-C

48608266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87536874-A-G

http://identifiers.org/hco/22/GRCh38#48608413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87537023-A-C

48608413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87537023-A-G

48611641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87538451-T-G

48611741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87538541-C-T

48611744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87538544-C-T

48611815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87538612-C-T

48612122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87540826-G-A

48612399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87541116-C-T

48612529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87541225-C-T

48612532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87541228-C-T

48614221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87542837-C-T

48614267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87542883-C-T

48614388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543005-A-T

48614548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543157-C-T

48614552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543165-C-T

48614554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543167-C-T

48614656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543285-C-T

http://identifiers.org/hco/22/GRCh38#48614682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87543309-A-C

48614682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543309-A-G

48614731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543365-C-G

48614731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543365-C-T

48614750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543392-C-T

48614759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543407-C-G

48614784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543427-G-T

48614879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543504-C-G

48614901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543541-G-T

48614902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543542-G-A

48614902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543542-G-T

48614930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543572-C-T

48614933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543575-C-T

48614934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543576-G-A

48614934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543576-G-C

48614989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543637-G-A

48615000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543657-G-A

48615103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543754-C-T

48615168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543825-G-A

48615178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543841-C-T

48615273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543925-C-G

48615273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543925-C-T

48615341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543964-G-A

48615353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87543978-G-A

48615468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87544061-G-C

48615660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87544239-C-T

48618422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87544914-G-A

48618449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87544941-G-T

48618550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87545037-C-T

48620256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87546236-G-A

48620290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87546253-C-T

48620563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87546537-T-C

48620734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87546839-T-C

48620854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87546952-C-T

48620872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87546972-A-G

48620956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87547046-C-G

http://identifiers.org/hco/22/GRCh38#48621017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87547097-A-C

48621017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87547097-A-G

http://identifiers.org/hco/22/GRCh38#48621075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87547155-A-C

48621075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87547155-A-T

http://identifiers.org/hco/22/GRCh38#48621136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87547216-A-C

48621136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87547216-A-T

48621146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87547226-C-T

48621155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87547234-T-C

http://identifiers.org/hco/22/GRCh38#48621216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87547293-C-A

48621248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87547323-A-G

http://identifiers.org/hco/22/GRCh38#48623141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87550031-C-A

48623569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87550321-G-A

48623871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87550622-C-T

48623948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87550702-T-C

48624058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87550796-C-T

48624104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87550847-G-A

48624305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87551035-C-T

http://identifiers.org/hco/22/GRCh38#48624360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87551092-A-C

48624388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87551120-A-G

48625289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87551576-T-G

48625457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87551750-A-G

48625457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87551750-A-T

48625969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87552154-C-T

48626003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87552187-A-G

48626022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87552209-G-T

48626092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87552269-C-G

48626246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87552418-G-T

48626542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87552664-G-A

48626542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87552664-G-T

48626767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87552882-A-G

http://identifiers.org/hco/22/GRCh38#48627015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87553134-C-A

48627015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87553134-C-T

48627100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87553209-A-G

48627506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87553591-T-C

48627758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87553811-G-A

http://identifiers.org/hco/22/GRCh38#48627790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87553825-C-A

48628459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87554445-C-T

48628581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87554520-C-T

48628582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87554521-G-A

48628599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87554545-A-G

48628838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87554767-C-T

48628893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87554814-G-C

48629424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87555266-C-G

48629424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87555266-C-T

48629934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87555717-G-A

48629934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87555717-G-T

48630254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87555944-G-A

48630361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556042-C-G

48630377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556054-G-A

48630526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556269-C-G

48630526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556269-C-T

48630930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556713-C-G

48630931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556714-G-A

48630931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556714-G-C

48631033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556806-G-A

48631040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556813-C-G

48631040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556813-C-T

48631062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556829-C-T

48631133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87556909-G-A

48636341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87561815-C-T

48636492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87561968-T-C

48644403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87563544-A-G

48644404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87563545-G-C

48644498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87563632-T-A

48644498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87563632-T-C

48644759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87563889-C-T

http://identifiers.org/hco/22/GRCh38#48644850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87563965-C-A

48644850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87563965-C-G

48644986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87564105-C-T

48645282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87564394-T-G

48645367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87564463-A-G

48645422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87564499-T-C

48645437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87564508-G-A

48645529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87564572-G-C

48645605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87564678-T-C

48645813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87564893-G-T

48646126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565281-G-A

48646157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565312-G-A

48646221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565356-A-G

48646227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565362-G-C

48646411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565541-G-A

48646498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565582-G-T

48646552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565634-G-A

48646768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565856-A-G

48646780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565868-G-A

48646780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87565868-G-T

48649921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87566901-C-T

48649966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87566947-G-A

48650071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567041-A-T

48650125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567098-G-A

48650163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567133-G-T

http://identifiers.org/hco/22/GRCh38#48650260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87567232-C-A

48650417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567408-T-C

48650477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567440-C-T

48650578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567526-G-T

http://identifiers.org/hco/22/GRCh38#48650609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87567555-A-C

48650929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567819-A-G

48650932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567822-A-G

48651042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567887-C-T

48651053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87567898-C-T

48651207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87568048-T-A

48651213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87568054-A-G

48654731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87571952-C-T

48654885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572108-T-C

48654907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572129-A-G

48654929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572147-C-T

48654985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572190-C-T

48655012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572216-T-C

48655398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572491-C-T

48655437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572527-C-T

48655535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572601-C-G

48655535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572601-C-T

48655562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572608-C-T

48655588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572634-A-G

48655652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572679-C-G

48655652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572679-C-T

http://identifiers.org/hco/22/GRCh38#48655677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87572703-C-A

48655716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572740-C-T

48655772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87572796-A-G

48657883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87575689-C-T

http://identifiers.org/hco/22/GRCh38#48658176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87575974-C-A

48658176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87575974-C-T

48658344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576082-C-T

48658356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576094-G-A

48658400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576159-G-T

48658401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576160-G-A

48658779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576541-G-A

48658956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576664-G-A

48658997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576705-G-A

http://identifiers.org/hco/22/GRCh38#48659081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87576786-A-C

48659202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576876-G-C

48659202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576876-G-T

48659284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87576947-G-T

48660335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87577732-C-T

48660391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87577787-G-A

48660517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87577914-A-G

48664387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579014-T-C

48664507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579131-A-G

48664536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579150-T-C

48664564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579177-A-T

48664753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579316-G-A

48664912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579462-C-T

http://identifiers.org/hco/22/GRCh38#48664937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87579490-A-C

48665031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579580-G-A

48665099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579647-G-A

48665217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579786-A-G

48665217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579786-A-T

48665350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579972-T-G

48665353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579975-T-C

48665378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87579999-C-G

48665445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580054-G-T

http://identifiers.org/hco/22/GRCh38#48665451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87580060-C-A

48665451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580060-C-T

http://identifiers.org/hco/22/GRCh38#48665466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87580074-A-C

48665466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580074-A-G

48665466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580074-A-T

48665512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580117-T-C

48665566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580170-A-G

48665809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580419-C-T

48665815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580423-G-A

48665815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580423-G-T

48665856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580460-T-C

48665948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580538-C-G

48666043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580611-G-T

48666300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580855-A-G

48666312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580867-C-T

48666364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87580902-T-G

48666627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581040-C-T

48666641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581051-A-G

http://identifiers.org/hco/22/GRCh38#48666706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87581104-C-A

48666878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581264-G-C

48666944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581341-G-A

48666946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581343-G-A

48666975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581371-G-C

48667225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581560-G-A

48667225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581560-G-C

48667386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87581692-A-G

http://identifiers.org/hco/22/GRCh38#48667693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87581996-C-A

48668901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87582118-G-T

48668968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87582191-G-A

http://identifiers.org/hco/22/GRCh38#48669125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87582323-C-A

http://identifiers.org/hco/22/GRCh38#48669175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87582369-C-A

48669239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87582431-G-A

48669342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87582577-C-G

48669445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87582722-C-T

48669741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87582991-C-T

48669776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583023-T-A

48669853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583067-T-C

48669904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583123-C-T

48669969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583144-T-C

48669979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583157-C-T

48670148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583353-T-C

48670497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583702-G-A

48670635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583828-T-C

48670761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583949-A-G

48670806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87583994-A-G

48671087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87584277-G-A

48671287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87584393-C-T

48671451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87584507-G-A

http://identifiers.org/hco/22/GRCh38#48671853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87584847-A-C

48671853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87584847-A-T

48671965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87584943-A-G

48671965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87584943-A-T

48672722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87585633-T-C

48672850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87585750-A-G

48672861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87585761-T-C

48672905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87585801-A-G

http://identifiers.org/hco/22/GRCh38#48672945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87585850-A-C

48672959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87585864-C-G

48672959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87585864-C-T

48674535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87586726-C-T

48686716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591149-G-C

48686716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591149-G-T

48686723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591156-T-A

48686869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591292-A-G

48686869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591292-A-T

http://identifiers.org/hco/22/GRCh38#48686940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87591351-A-C

48686940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591351-A-G

48686941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591352-T-G

48687253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591625-A-G

48687269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591641-A-G

48687331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591693-G-A

48687339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591701-A-G

48687442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591776-C-G

48687442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591776-C-T

48687561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591892-C-T

48687679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87591999-C-G

48687833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87592125-C-T

48688071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87592352-G-T

48688168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87592424-C-G

48696429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87594656-C-G

48696761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87594960-C-T

48698066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87595386-A-G

48698089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87595407-G-A

48698089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87595407-G-T

48698337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

48698340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

48698380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

48698427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

48698840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87596065-C-T

http://identifiers.org/hco/22/GRCh38#48698973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

48698973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/22/GRCh38#48698974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

48699053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

48699152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

48699152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/22/GRCh38#48699234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

48699234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

48699234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

48699309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87596273-A-G

48702467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87599330-T-C

48702483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87599348-G-A

48702556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87599403-C-T

48702889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87599728-C-T

48702966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87599795-G-T

48704330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87601311-C-T

48704542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87601498-C-T

48704668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87601601-T-A

48704669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87601602-G-T

48704679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87601623-G-A

48704852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87601764-A-G

48704852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87601764-A-T

http://identifiers.org/hco/22/GRCh38#48704932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87601827-C-A

48705163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87602009-C-T

http://identifiers.org/hco/22/GRCh38#48705575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87602374-C-A

48705739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87602521-A-G

48705739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87602521-A-T

48705741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87602523-G-A

48705748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87602530-G-A

48705799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87602591-G-A

48707647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87604620-G-A

48707881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87604868-G-T

48707886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87604895-G-A

48707886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87604895-G-C

48707886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87604895-G-T

48707889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87604898-A-G

48707889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87604898-A-T

48707903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87604912-C-T

48708158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87605109-G-A

48708198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87605153-T-A

48708201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87605156-G-A

48708203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87605158-C-T

48708348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87605285-C-T

48711500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87606301-G-A

http://identifiers.org/hco/22/GRCh38#48711794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87606553-A-C

http://identifiers.org/hco/22/GRCh38#48711846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87606585-A-C

http://identifiers.org/hco/22/GRCh38#48712563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87606956-A-C

48712563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87606956-A-G

48712581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87606974-G-A

http://identifiers.org/hco/22/GRCh38#48712611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87607005-C-A

48712611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607005-C-T

48712731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607135-C-T

48712888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607284-C-T

48712921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607319-G-A

48712921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607319-G-C

48713061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607459-C-T

48713182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607579-G-A

48713381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607733-G-A

48713381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607733-G-T

48713443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607768-G-A

48713443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607768-G-T

48713692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607992-G-A

48713696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87607996-C-T

48713756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87608059-C-T

48719292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87610792-G-A

48719352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87610850-G-A

48719353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87610851-G-A

http://identifiers.org/hco/22/GRCh38#48719408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87610929-A-C

48719428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87610949-T-A

48719428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87610949-T-C

48719461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87610984-G-A

48719461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87610984-G-T

48719762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87611302-C-T

http://identifiers.org/hco/22/GRCh38#48719895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87611433-C-A

48719980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87611521-G-A

48720046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87611586-A-G

http://identifiers.org/hco/22/GRCh38#48720158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87611700-C-A

48720158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87611700-C-T

48720168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87611725-G-A

48720172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87611729-T-A

http://identifiers.org/hco/22/GRCh38#48720197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87611782-A-C

48720206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87611791-A-G

48720300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87611953-C-T

48720419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612083-A-G

48720603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612234-C-T

48720615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612244-G-T

48720619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612248-G-A

http://identifiers.org/hco/22/GRCh38#48720681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87612305-C-A

48720681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612305-C-T

48720929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612522-T-C

48721098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612654-G-A

48721107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612663-A-G

48723147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87612973-G-A

48723198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87613012-C-T

48723243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87613059-C-T

48723280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87613987-G-A

48723656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87614328-A-T

48723867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87614476-T-C

48724328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87614709-G-A

48724328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87614709-G-T

48724336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87614717-T-C

48724437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87614814-G-A

48724545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87614888-G-A

48724935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87615199-G-A

48725551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87615725-G-A

http://identifiers.org/hco/22/GRCh38#48725681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87615854-C-A

http://identifiers.org/hco/22/GRCh38#48725707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87615879-C-A

48725834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87615971-G-A

48725920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87616074-A-G

48725936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87616090-A-G

http://identifiers.org/hco/22/GRCh38#48725951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87616100-C-A

http://identifiers.org/hco/22/GRCh38#48726090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87616232-C-A

48727160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87616480-A-G

48727357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87616733-G-A

48727357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87616733-G-C

48727373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87616765-G-C

48727586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87616966-T-C

48727665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87617044-A-G

48727783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87617159-A-G

48727867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87617256-G-A

48728428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87617678-G-A

48728660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87617880-G-A

48728663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87617883-T-C

48728753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87617983-A-G

48728824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87618042-C-T

48728881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87618105-A-G

48729074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87618280-C-T

48729075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87618281-A-G

48729081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87618285-G-T

48734641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87619532-A-G

48734687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87619581-T-C

48734743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87619628-C-T

http://identifiers.org/hco/22/GRCh38#48734744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87619629-C-A

48734778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87619656-G-A

48734847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87619707-G-A

48735485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87620416-C-T

48735653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87620567-T-A

48735754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87620658-G-C

48749904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641565-T-A

48749904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641565-T-C

http://identifiers.org/hco/22/GRCh38#48749910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641571-C-A

48749910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641571-C-T

http://identifiers.org/hco/22/GRCh38#48749927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641588-C-A

http://identifiers.org/hco/22/GRCh38#48749928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641589-C-A

48749928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641589-C-T

http://identifiers.org/hco/22/GRCh38#48749971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641630-C-A

48749971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641630-C-T

http://identifiers.org/hco/22/GRCh38#48750109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641768-C-A

48750109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641768-C-T

48750178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641811-T-C

48750178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641811-T-G

http://identifiers.org/hco/22/GRCh38#48750179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641812-C-A

48750179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641812-C-G

http://identifiers.org/hco/22/GRCh38#48750196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641826-C-A

48750196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641826-C-T

http://identifiers.org/hco/22/GRCh38#48750204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641834-C-A

http://identifiers.org/hco/22/GRCh38#48750247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87641875-C-A

48750263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641891-T-G

48750275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87641903-G-T

48750394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87642023-G-A

48750394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87642023-G-T

http://identifiers.org/hco/22/GRCh38#48750395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87642024-C-A

48750395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87642024-C-G

48750395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87642024-C-T

http://identifiers.org/hco/22/GRCh38#48750405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87642034-A-C

48750405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87642034-A-G

http://identifiers.org/hco/22/GRCh38#48750469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87642096-A-C

48750469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87642096-A-T

48750485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87642113-G-C

48750485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87642113-G-T

48750888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642540-G-A

48750888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642540-G-T

48750946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642600-G-T

48750982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642616-C-T

48751031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642661-G-A

48751108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642716-C-T

48751217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642814-T-C

http://identifiers.org/hco/22/GRCh38#48751269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87642872-C-A

48751269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642872-C-T

48751373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87642964-T-C

48751548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87643170-G-A

48751548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87643170-G-T

http://identifiers.org/hco/22/GRCh38#48751766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87643400-C-A

48751766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87643400-C-T

http://identifiers.org/hco/22/GRCh38#48751776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87643409-C-A

48751776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87643409-C-G

48751776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87643409-C-T

48752033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87643666-G-A

48752069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87643693-G-T

48752355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87643991-C-G

48752464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87644091-C-T

48756282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87645812-G-A

48756355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87645885-G-T

48756482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87646009-G-A

http://identifiers.org/hco/22/GRCh38#48756552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87646078-C-A

48759457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648398-G-A

48759510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648422-G-A

48759569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648481-C-G

48759584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648496-C-T

48759683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648561-A-G

48759690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648568-C-G

48759922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648710-G-A

48760047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648783-C-T

48760099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648817-C-T

48760248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648938-T-C

48760311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87648992-G-A

48760503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649177-G-A

48760696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649348-A-G

48760786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649435-T-C

48760906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649545-G-A

48760966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649609-G-T

48761077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649692-A-G

48761131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649709-C-T

48761134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649712-G-A

48761268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649805-G-A

48761268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649805-G-C

48761386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87649932-A-T

48761668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650200-G-A

48761681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650213-G-A

48761828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650350-A-G

48761835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650356-G-A

48761835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650356-G-T

48761911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650417-C-T

48762012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650516-C-G

48762012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650516-C-T

http://identifiers.org/hco/22/GRCh38#48762138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87650615-A-C

48762155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650632-C-G

48762155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87650632-C-T

48762422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87651046-C-G

http://identifiers.org/hco/22/GRCh38#48762582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87651235-A-C

48763318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87651961-G-T

48763546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87652170-T-C

48763605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87652223-G-A

48763645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87652264-A-G

48778703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87667781-G-A

48778703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87667781-G-C

48778703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87667781-G-T

48778734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87667814-C-T

http://identifiers.org/hco/22/GRCh38#48779073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87668179-C-A

48779073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87668179-C-T

http://identifiers.org/hco/22/GRCh38#48779092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87668199-C-A

48779273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87668391-G-A

48779592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87669574-T-C

48779602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87669585-C-G

48779626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87669609-G-A

48782323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87670670-T-C

48782326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87670673-C-T

48782351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87670703-C-T

48782761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87671105-T-C

http://identifiers.org/hco/22/GRCh38#48782804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87671148-C-A

48782901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87671259-G-A

48783514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87671556-C-T

48804535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87679670-C-T

http://identifiers.org/hco/22/GRCh38#48804606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87679744-C-A

48804606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87679744-C-G

48804606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87679744-C-T

48804617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87679755-G-A

48804788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87679912-G-A

48804788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87679912-G-C

48804844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87679982-C-T

48804974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87680108-G-A

48804974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87680108-G-T

48806656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87680997-G-A

48806688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681031-G-T

48806777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681089-G-A

48806932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681199-G-A

48806932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681199-G-C

48807019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681280-C-T

48807026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681287-A-G

48807124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681370-C-T

48807451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681739-G-A

48807451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681739-G-C

48807560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681868-C-G

48807690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87681978-G-A

48807834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87682128-T-A

48807834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87682128-T-C

48807844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87682138-G-A

48807986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87682283-A-T

48807987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87682284-G-T

48807988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87682285-A-T

http://identifiers.org/hco/22/GRCh38#48807994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87682291-C-A

48808005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87682307-T-C

48820393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87693775-T-C

48820412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87693794-A-G

48820705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87694060-T-C

48820755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87694119-G-A

48820757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87694121-G-C

48820757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87694121-G-T

48820767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87694131-G-T

48821460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87695109-A-T

48823855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87696178-G-A

48823948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87696265-C-T

48824016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87696325-G-A

http://identifiers.org/hco/22/GRCh38#48824584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87696914-A-C

48824689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697017-C-T

http://identifiers.org/hco/22/GRCh38#48824916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87697248-C-A

48824924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697256-C-T

48824927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697259-T-C

http://identifiers.org/hco/22/GRCh38#48825068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87697376-A-C

http://identifiers.org/hco/22/GRCh38#48825085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87697393-C-A

48825085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697393-C-T

48825111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697409-T-G

48825225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697498-C-T

48825345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697608-A-G

48825486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697746-A-G

48825574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697822-T-G

48825722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697900-G-T

48825745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697915-T-C

48825757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697929-A-G

48825789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87697969-C-T

48825898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698058-T-C

48826009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698150-G-A

48826009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698150-G-T

48826011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698152-C-T

48826012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698153-G-A

48826012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698153-G-T

48826063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698282-C-T

48826064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698283-G-A

48826266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698491-T-A

48826322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698564-G-A

48826339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698603-C-T

48826354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698616-T-C

48826354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698616-T-G

48826423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698665-C-T

48826670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698887-G-A

48826687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698904-G-T

48826741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698954-G-A

48826747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698958-C-G

48826747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87698958-C-T

48827393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699175-T-G

48827522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699307-T-G

48827636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699412-G-A

48827642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699426-G-A

48827808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699575-G-A

48828069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699832-G-A

48828151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699870-A-G

48828151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699870-A-T

48828286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699970-G-A

48828365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700039-G-A

48828382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700053-T-C

48828425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700096-G-A

48828449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700117-C-G

http://identifiers.org/hco/22/GRCh38#48828657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87700301-A-C

48828700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700364-G-T

48828721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700385-C-G

48828750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700417-C-T

48828776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700442-C-T

48828814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700481-G-A

48828814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700481-G-T

48828826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700489-G-A

http://identifiers.org/hco/22/GRCh38#48828838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87700494-C-A

48828851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87700507-G-A

http://identifiers.org/hco/22/GRCh38#48830258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87699787-A-C

48830258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87699787-A-G

48838012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87702797-A-G

48838102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87702894-C-T

48838323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87703108-G-T

48838436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87703222-T-C

http://identifiers.org/hco/22/GRCh38#48838472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87703259-A-C

48838489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87703269-G-A

48838553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87703315-T-G

48838610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87703382-T-C

48838642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87703415-A-G

http://identifiers.org/hco/22/GRCh38#48844761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87707716-C-A

http://identifiers.org/hco/22/GRCh38#48844790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#87707750-C-A

48845744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21592
most severe consequence: intron variant
orthologous variants: 87708235-C-T