47206713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 3 prime UTR variant
orthologous variants: 76988181-T-C

47207046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76987245-C-T

47207048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76987243-G-A

47207084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76987214-C-T

47207135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76987163-G-C

47207190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76987110-G-T

47207208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76987093-T-C

47207208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76987093-T-G

47207226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76987067-G-A

47207426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76986886-C-T

47207498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76986855-C-T

47207510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76986843-G-C

47207637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76986713-A-G

47207769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76986620-G-A

47207769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76986620-G-T

47208107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76986038-A-G

47208108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76986037-G-A

47208180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76985954-C-T

47208327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76985817-C-G

47208702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76985423-C-T

47209154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76984731-A-G

47209718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76984186-A-T

47210234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76983988-G-T

47210477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76983812-T-C

47210564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76983734-C-G

47210651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76983651-T-C

47210962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76983372-C-T

47211216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76983150-G-A

47211216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76983150-G-C

47211363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76982644-T-C

47211529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76982477-T-G

47211572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76982423-C-T

47211622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76982376-G-A

47211662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76982338-C-G

47211687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76982299-T-G

47211827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76982108-C-T

47211951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76981984-A-G

http://identifiers.org/hco/18/GRCh38#47211994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76981941-C-A

47211994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76981941-C-G

47212047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76981891-C-G

47212047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76981891-C-T

http://identifiers.org/hco/18/GRCh38#47212062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76981876-A-C

47212062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76981876-A-G

47212070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76981868-C-T

47212078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76981860-G-A

47212108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense variant
orthologous variants: 76981829-G-T

47212264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76981693-A-G

http://identifiers.org/hco/18/GRCh38#47212268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76981689-A-C

47213301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76980760-T-C

47213485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76980449-C-T

http://identifiers.org/hco/18/GRCh38#47213605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76980356-A-C

47214092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979911-C-T

47214169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979834-G-A

47214286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979704-T-G

47214339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979684-A-G

http://identifiers.org/hco/18/GRCh38#47214469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76979554-C-A

47214481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979543-A-G

47214561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979493-A-T

47214569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979488-A-G

47214590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979466-A-T

47214733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979303-T-C

47214802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979237-A-G

47215056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76979001-G-C

47215078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76978979-G-C

47215165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76978903-G-A

47215352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76978719-C-T

47215461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76978666-C-T

http://identifiers.org/hco/18/GRCh38#47215695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76978461-C-A

47215835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76978320-T-C

47215926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76978246-A-G

47215927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76978245-T-C

47216094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76978093-C-T

47216289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977934-T-A

http://identifiers.org/hco/18/GRCh38#47216312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76977911-A-C

47216415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977807-C-T

47216489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977727-A-T

http://identifiers.org/hco/18/GRCh38#47216497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76977719-A-C

47216497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977719-A-T

47216498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977718-G-A

47216498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977718-G-C

47216814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977406-G-C

47216855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977364-A-G

47217057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977169-C-T

47217078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977148-C-T

47217094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76977132-A-G

47217281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976980-T-C

47217351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976914-T-C

47217562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976741-T-C

47217562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976741-T-G

47217739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976615-G-A

47218051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976343-G-A

47218214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976196-C-G

47218214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976196-C-T

47218269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976141-G-A

47218623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976104-G-T

47218672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976053-G-A

47218703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76976024-G-A

47218771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975956-T-A

47218771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975956-T-C

47218803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975895-C-T

http://identifiers.org/hco/18/GRCh38#47218824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76975874-A-C

47218837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975861-A-G

47218871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975743-T-A

47218908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975706-G-T

47219032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975507-A-G

47219296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975258-A-G

47219308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975246-G-A

http://identifiers.org/hco/18/GRCh38#47219467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76975114-C-A

47219467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76975114-C-T

47219660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76974933-T-C

47219747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76974847-C-T

47219790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76974804-A-G

47219881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76974720-T-C

47219881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76974720-T-G

47219914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76974687-A-G

47220013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76974589-G-A

47220013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76974589-G-T

47220063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76974539-T-C

47220973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76972893-C-T

47221005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76972862-T-C

47221138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76972734-G-C

47221186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76972695-T-C

47221433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76972293-T-G

47221656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76972081-C-T

47221664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76972073-A-G

47221853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76971937-G-A

47222396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76971717-T-C

47222408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76971705-G-A

http://identifiers.org/hco/18/GRCh38#47222564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76971543-A-C

http://identifiers.org/hco/18/GRCh38#47222583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76971524-C-A

47222615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76971493-C-T

http://identifiers.org/hco/18/GRCh38#47222627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76971482-C-A

47222729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76971252-G-T

47222759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76971216-T-C

47222789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76971187-C-G

47222950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76971037-G-A

http://identifiers.org/hco/18/GRCh38#47223128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76970698-A-C

47223468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76970353-C-G

47223479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76970342-A-G

47225680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76968462-T-G

47225812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76968342-G-A

47225814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76968340-C-T

47225958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76968200-T-C

http://identifiers.org/hco/18/GRCh38#47226007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76968148-A-C

47227890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76967358-C-T

47227926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76967322-A-G

47228110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76967145-T-C

47228222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76967039-T-A

47228526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76966342-A-G

47230139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76964664-T-C

http://identifiers.org/hco/18/GRCh38#47230244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76964533-C-A

47230357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76964432-T-C

47230357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76964432-T-G

47230368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76964419-A-G

47230401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76964388-T-C

47230448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76964342-T-C

47230461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 76964329-A-G

47230610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76964176-A-G

47230624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76964162-T-C

47230869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76963917-C-T

47230918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76963869-T-A

47231012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76963775-G-T

47231026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76963761-A-G

47231080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76963711-T-A

http://identifiers.org/hco/18/GRCh38#47231187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76963597-A-C

47231187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76963597-A-G

47231204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76963580-C-T

47231216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76963568-G-A

47232704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962799-T-C

47232731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962769-C-T

47233033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962466-G-A

47233060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962439-T-C

47233063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962436-G-A

47233080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962419-C-T

47233202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962291-A-G

47233242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962253-C-T

47233449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962061-G-C

47233462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962048-G-A

47233462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76962048-G-T

47233680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76961853-T-C

47233699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76961834-A-T

47233715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76961820-C-T

47234396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76961120-A-G

47234877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76961065-A-G

47234877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76961065-A-T

http://identifiers.org/hco/18/GRCh38#47235770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76960590-C-A

http://identifiers.org/hco/18/GRCh38#47235803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76960571-A-C

47235814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76960560-T-A

47236278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76960398-A-G

47236292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76960384-A-T

http://identifiers.org/hco/18/GRCh38#47236342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76960332-C-A

47236492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76960158-C-T

47237148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76959667-C-G

47237148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76959667-C-T

47237549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76957819-T-G

47237580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76957769-G-A

47237588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76957761-G-A

47238863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76957263-C-T

47239070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76957070-T-C

47239092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76957048-G-T

47239412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76956547-T-A

47239611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76956193-G-A

47239712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76955931-A-G

47240231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76955399-G-C

47240729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76954965-A-G

47240827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76954864-T-C

47240928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76954759-G-C

47240931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76954756-A-G

47240995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76954695-G-C

47241002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76954688-G-C

47241782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76953553-A-G

47241945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76953390-T-G

47242041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76953260-T-A

47242054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76953247-T-A

47242288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76953007-G-A

47242519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76952797-A-T

47242683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76952625-T-A

http://identifiers.org/hco/18/GRCh38#47242838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76952468-C-A

47242921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76952375-T-C

47243145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76952170-T-C

47243172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76952143-G-A

47243915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76951402-A-G

47244072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76951245-T-A

47244075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76951242-T-C

47244834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950473-G-T

47244854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950456-A-G

47244854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950456-A-T

http://identifiers.org/hco/18/GRCh38#47245019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76950294-C-A

47245042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950271-G-A

47245042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950271-G-C

47245042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950271-G-T

http://identifiers.org/hco/18/GRCh38#47245043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76950270-A-C

47245043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950270-A-G

47245043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950270-A-T

http://identifiers.org/hco/18/GRCh38#47245068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76950260-A-C

47245068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950260-A-G

47245068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950260-A-T

47245071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950257-A-G

47245071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950257-A-T

http://identifiers.org/hco/18/GRCh38#47245077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76950249-C-A

47245077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950249-C-G

47245077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950249-C-T

47245081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950245-T-C

47245082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950244-T-A

http://identifiers.org/hco/18/GRCh38#47245105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76950221-A-C

47245113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950213-G-A

47245113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76950213-G-T

47245414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76949932-G-T

47245418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76949926-A-G

47245476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76949870-T-A

47245476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76949870-T-C

47245476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76949870-T-G

47245738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76949611-T-G

47245771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76949581-C-T

http://identifiers.org/hco/18/GRCh38#47246444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76949002-A-C

47246689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948757-T-C

http://identifiers.org/hco/18/GRCh38#47246862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76948581-C-A

47246862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948581-C-G

47246862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948581-C-T

47247049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948394-T-C

47247049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948394-T-G

47247070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948373-G-A

47247070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948373-G-C

47247070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948373-G-T

http://identifiers.org/hco/18/GRCh38#47247105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76948347-C-A

47247105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948347-C-G

47247105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948347-C-T

47247179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948273-G-A

47247179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948273-G-C

47247179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948273-G-T

47247187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948265-T-A

47247187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948265-T-C

47247187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948265-T-G

47247229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 76948226-G-A

47247229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 76948226-G-T

47247307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948148-G-A

47247307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948148-G-C

47247307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948148-G-T

http://identifiers.org/hco/18/GRCh38#47247340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#76948115-C-A

47247340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 76948115-C-T

47247435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948020-G-A

47247435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948020-G-C

47247435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948020-G-T

http://identifiers.org/hco/18/GRCh38#47247556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#76947902-C-A

47247556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 76947902-C-T

47247598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 76947860-G-A

47247598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 76947860-G-C

47247598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 76947860-G-T

http://identifiers.org/hco/18/GRCh38#47247614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/18/GRCm39#76947844-C-A

47247614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947844-C-G

47247614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947844-C-T

47247700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947758-A-G

http://identifiers.org/hco/18/GRCh38#47247742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#76947716-A-C

47247742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 76947716-A-G

http://identifiers.org/hco/18/GRCh38#47247871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76947587-C-A

47247871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947587-C-T

47247925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947533-A-G

http://identifiers.org/hco/18/GRCh38#47247928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76947530-C-A

47247928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947530-C-G

47247928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947530-C-T

47248046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947412-A-G

47248138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947320-C-T

47248192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947266-G-A

47248192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947266-G-T

47248240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947218-T-C

47248291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947167-A-G

47248291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947167-A-T

47248324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947137-G-A

47248324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947137-G-T

47248327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947134-G-A

47248327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947134-G-T

http://identifiers.org/hco/18/GRCh38#47248360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76947101-C-A

47248360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947101-C-G

47248360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron_variant, missense_variant
orthologous variants: 76947101-C-T

http://identifiers.org/hco/18/GRCh38#47248408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76947053-A-C

http://identifiers.org/hco/18/GRCh38#47248687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76946774-C-A

47248687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense variant
orthologous variants: 76946774-C-T

http://identifiers.org/hco/18/GRCh38#47249011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76946450-C-A

47249011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense variant
orthologous variants: 76946450-C-G

47249011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense variant
orthologous variants: 76946450-C-T

47249095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense variant
orthologous variants: 76946366-C-G

47249095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: missense variant
orthologous variants: 76946366-C-T

http://identifiers.org/hco/18/GRCh38#47249097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76946364-C-A

47249353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76946109-G-C

47250514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944918-A-T

47250824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944647-C-G

47250842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944629-T-C

47250842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944629-T-G

47250962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944511-G-T

47251129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944351-T-A

47251129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944351-T-G

47251151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944329-T-A

47251151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944329-T-C

47251151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944329-T-G

47251360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: intron variant
orthologous variants: 76944145-G-A

47251404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 5 prime UTR variant
orthologous variants: 76944101-G-T

http://identifiers.org/hco/18/GRCh38#47251409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76944096-C-A

47251409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 5 prime UTR variant
orthologous variants: 76944096-C-T

47251487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 5 prime UTR variant
orthologous variants: 76944018-C-T

47251519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 5 prime UTR variant
orthologous variants: 76943988-G-C

47251519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 5 prime UTR variant
orthologous variants: 76943988-G-T

47251563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32695
most severe consequence: 5 prime UTR variant
orthologous variants: 76943935-T-C