11632324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66022142-G-A

11632334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66022132-G-T

11632355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66022108-A-G

11632466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021624-A-G

http://identifiers.org/hco/17/GRCh38#11632554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66021537-C-A

11632554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021537-C-G

11632554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021537-C-T

11632555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021536-G-A

11632555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021536-G-T

11632572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021519-A-G

11632715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021376-T-G

11632719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021372-G-A

11632719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021372-G-T

http://identifiers.org/hco/17/GRCh38#11632748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66021349-C-A

11632748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021349-C-G

11632748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021349-C-T

11632816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021305-T-G

11632994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66021148-G-A

11633380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66020776-C-G

11633380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66020776-C-T

11633459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66020705-T-C

11633575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66020593-T-G

11633715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66020472-G-A

http://identifiers.org/hco/17/GRCh38#11633902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66020353-C-A

11633902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66020353-C-G

11634484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66019793-C-T

11634761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66019201-C-T

11634881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66019075-C-G

11634881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66019075-C-T

11635148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66018788-T-C

11636609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66017598-T-C

11636928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66017275-A-G

11637009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66017189-G-A

11639297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66016678-C-G

11639297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66016678-C-T

11639545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66016444-A-G

11640053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66016228-G-T

11640121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66016174-G-T

11640308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 66016013-G-A

11640341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 66015980-C-T

11641114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66015328-C-T

http://identifiers.org/hco/17/GRCh38#11642713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66014134-A-C

11642800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66014052-C-T

11642815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66014037-A-G

11642834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66014023-C-T

11642966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66013912-C-T

11642992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66013887-G-A

11643177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66013706-G-A

11643365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66013505-T-G

11644325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, undefined
orthologous variants: 66013156-G-A

11644325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, undefined
orthologous variants: 66013156-G-C

11644385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, undefined
orthologous variants: 66013094-T-C

11644530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012945-G-T

11644725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012624-G-A

11644725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012624-G-C

11644725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012624-G-T

11644728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012621-T-A

11644728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012621-T-C

http://identifiers.org/hco/17/GRCh38#11644742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66012564-C-A

11644742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012564-C-T

http://identifiers.org/hco/17/GRCh38#11644746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66012560-C-A

11644746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012560-C-G

11644778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012521-G-T

11644787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012512-G-T

11644788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012511-T-A

11644788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012511-T-C

http://identifiers.org/hco/17/GRCh38#11644825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66012474-C-A

11644855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012442-T-C

11645158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012160-A-G

11645167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66012151-G-T

11645559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66011756-C-T

11646356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66011481-G-A

11646358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66011479-T-A

11646797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66011053-C-G

11647091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant
orthologous variants: 66010526-G-A

http://identifiers.org/hco/17/GRCh38#11647142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66010475-C-A

11647230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66010387-T-A

11647230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66010387-T-C

11647230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66010387-T-G

11650960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66009900-A-G

11651368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66009493-G-A

11651368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66009493-G-C

11651368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66009493-G-T

11651423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66009432-G-T

11651479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66009377-A-G

11651749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66009100-A-G

http://identifiers.org/hco/17/GRCh38#11652623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66008614-C-A

11652644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008593-G-A

11652644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008593-G-T

11652645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008592-T-A

11652645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008592-T-C

11652645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008592-T-G

http://identifiers.org/hco/17/GRCh38#11652665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66008572-C-A

11652665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008572-C-T

11652666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008571-T-C

http://identifiers.org/hco/17/GRCh38#11652671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66008566-A-C

11652671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008566-A-G

11652685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008553-G-A

11652701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008537-A-G

11652701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008537-A-T

http://identifiers.org/hco/17/GRCh38#11652718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66008520-A-C

11652718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008520-A-G

11652719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66008519-C-T

11653420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66007872-G-A

11653755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66007571-A-G

11664048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66004059-C-T

11664140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003967-T-G

11664482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003547-C-G

11664700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003332-G-A

11664700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003332-G-T

11664758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003283-T-C

11664786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003258-T-C

11664797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003247-A-G

http://identifiers.org/hco/17/GRCh38#11664800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66003244-C-A

11664800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003244-C-T

11664801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003243-G-A

11664801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003243-G-T

11664821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003223-T-C

http://identifiers.org/hco/17/GRCh38#11665012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66003032-C-A

11665012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003032-C-G

11665012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66003032-C-T

11665257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66002826-G-T

11665341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66002750-G-A

11665518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66002582-G-A

11666171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66002003-G-A

11666230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66001946-G-A

http://identifiers.org/hco/17/GRCh38#11666274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66001905-C-A

11666274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66001905-C-G

11666625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66001541-A-G

http://identifiers.org/hco/17/GRCh38#11666942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66001278-A-C

11667127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66001091-A-G

11667176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66001042-A-G

11667933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66000164-G-A

11668088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 66000013-T-C

11668231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65999899-G-T

11668286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65999896-C-T

11668694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65999762-T-A

11668759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65999686-T-G

11669034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65999434-T-A

11669243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65999231-G-C

11669305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65999187-A-G

11669315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65999177-C-T

http://identifiers.org/hco/17/GRCh38#11669368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: splice acceptor variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65999124-A-C

11669409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65999083-C-T

11669631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65998861-T-G

11669656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65998836-T-C

11669822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65998670-A-G

http://identifiers.org/hco/17/GRCh38#11669843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65998650-C-A

http://identifiers.org/hco/17/GRCh38#11669877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65998600-C-A

11669877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65998600-C-T

http://identifiers.org/hco/17/GRCh38#11669942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65998542-C-A

11669942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65998542-C-T

11670561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997933-C-T

11670574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997920-C-G

11671197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997603-A-T

11671437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997426-T-A

11671574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997317-A-G

11671718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997185-T-C

11671739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997163-G-A

11671747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997155-A-G

11671747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65997155-A-T

11671921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996987-C-T

11671941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996984-A-G

11672074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996846-C-G

11672210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996708-A-T

11672240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996678-A-G

11672243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996661-C-T

11672296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996601-C-G

11672449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996400-T-A

11672531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996321-G-A

11672687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996193-C-T

11672781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65996105-T-G

11673007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65995897-T-C

11673011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65995893-C-T

http://identifiers.org/hco/17/GRCh38#11673130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65995783-A-C

11679564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65986449-C-T

11679614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65986404-A-G

11679614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65986404-A-T

11679645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65986386-G-A

11679645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65986386-G-T

11679693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65986341-A-T

11679770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65986270-G-T

11679938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65986102-T-G

11679965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65986075-T-G

11680219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985827-G-T

11680508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985208-T-G

11680555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985155-G-A

11680621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985098-T-C

11680662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985054-A-G

11680677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985039-G-A

11680677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985039-G-T

11680701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985017-C-T

11680710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985008-G-A

11680710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985008-G-C

11680710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65985008-G-T

11680765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65984953-A-G

11680771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: stop gained
orthologous variants: 65984947-A-T

11680820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65984898-A-G

11680834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65984884-T-C

http://identifiers.org/hco/17/GRCh38#11680869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65984849-C-A

11680892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65984826-A-G

11680942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65984815-T-C

11681033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65984723-A-T

11681054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65984702-G-A

11683782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65983051-C-T

11683968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65982884-G-C

http://identifiers.org/hco/17/GRCh38#11684829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65982173-C-A

http://identifiers.org/hco/17/GRCh38#11685033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65981962-C-A

11686409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65980800-C-T

11686443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65980768-C-G

11686443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65980768-C-T

11686474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65980739-C-T

11686809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65980343-T-C

11687339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65979664-G-A

11687591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65979442-C-G

11687591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65979442-C-T

http://identifiers.org/hco/17/GRCh38#11689466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65976407-C-A

http://identifiers.org/hco/17/GRCh38#11689489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65976383-C-A

11689546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65976328-G-A

11689546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65976328-G-C

http://identifiers.org/hco/17/GRCh38#11689606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65976268-C-A

11689945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65975929-G-A

11689945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65975929-G-C

11690194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65975680-A-G

http://identifiers.org/hco/17/GRCh38#11690331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65975543-C-A

11690389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65975485-G-A

11690389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65975485-G-C

11690734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65975141-A-G

11690841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65975031-C-G

11690905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65974967-A-G

11691133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65974752-G-T

11692266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65973994-T-C

11692391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65973861-G-A

11692391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65973861-G-C

11692396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65973853-T-C

http://identifiers.org/hco/17/GRCh38#11692436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65973826-A-C

11692437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65973825-G-A

11692561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65973790-C-T

11693626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65972370-T-C

11693728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65972313-T-G

11693855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65972221-T-C

http://identifiers.org/hco/17/GRCh38#11693924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65972152-C-A

11693943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65972133-G-A

http://identifiers.org/hco/17/GRCh38#11694057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65972026-C-A

11694057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65972026-C-G

11694057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65972026-C-T

11694157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65971923-C-T

11694164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65971916-G-T

11694218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65971862-T-C

11694281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65971485-G-A

11694297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65971469-A-G

11694346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65971420-G-A

11694346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65971420-G-C

11694346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65971420-G-T

11694353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65971413-A-G

11694481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65971287-G-A

http://identifiers.org/hco/17/GRCh38#11694482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65971286-A-C

11694491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65971277-G-A

11694493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65971275-G-T

11697547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65967986-A-T

11697691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65967851-T-C

11697801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65967758-T-G

11697847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65967722-G-C

http://identifiers.org/hco/17/GRCh38#11699622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65967391-C-A

11699622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65967391-C-T

11699687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65967330-C-T

11699737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65967282-C-T

11699861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65967158-A-G

http://identifiers.org/hco/17/GRCh38#11699991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65967037-C-A

11699991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65967037-C-T

11700031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65967020-A-G

http://identifiers.org/hco/17/GRCh38#11700079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65966977-A-C

11700193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65966867-C-G

11700193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65966867-C-T

11700381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65966699-C-T

11700536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65966544-G-A

http://identifiers.org/hco/17/GRCh38#11700970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65966141-C-A

11700970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65966141-C-T

11701010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65966106-T-C

11701143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65965972-G-A

http://identifiers.org/hco/17/GRCh38#11701221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65965894-C-A

11701221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: stop gained
orthologous variants: 65965894-C-T

http://identifiers.org/hco/17/GRCh38#11701267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65965848-C-A

11701267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965848-C-T

http://identifiers.org/hco/17/GRCh38#11701268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65965847-C-A

11701268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965847-C-G

http://identifiers.org/hco/17/GRCh38#11701308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65965802-C-A

11701308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965802-C-T

11701362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965745-G-A

11701398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965710-G-C

11701398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965710-G-T

11701408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965701-G-T

11701418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965691-C-T

http://identifiers.org/hco/17/GRCh38#11701530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65965594-A-C

http://identifiers.org/hco/17/GRCh38#11701535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65965590-C-A

11701537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965588-A-G

11702330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965199-C-T

11702363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965160-C-G

11702363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965160-C-T

11702369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965154-G-A

11702422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65965101-G-T

11702544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65964981-G-C

11702602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65964927-C-T

11702615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65964914-T-A

11703607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65964363-C-T

http://identifiers.org/hco/17/GRCh38#11703623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65964349-A-C

11703823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65964170-G-A

11703829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65964164-T-C

11704135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65963872-G-A

11704135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65963872-G-T

11704416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65963591-G-A

11704446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963561-G-A

11704446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963561-G-T

11704479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963529-T-C

11704510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963503-A-G

11704554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963469-T-A

11704554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963469-T-G

11704559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963464-G-A

11704559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963464-G-T

http://identifiers.org/hco/17/GRCh38#11704578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65963445-C-A

11704578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963445-C-G

11704578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963445-C-T

http://identifiers.org/hco/17/GRCh38#11704859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65963119-A-C

http://identifiers.org/hco/17/GRCh38#11704877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65963080-C-A

11704877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963080-C-T

11704898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963060-T-C

11704908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963050-A-G

http://identifiers.org/hco/17/GRCh38#11704916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65963042-C-A

11704916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963042-C-T

11704941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65963017-G-T

http://identifiers.org/hco/17/GRCh38#11704969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65962989-C-A

11704969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65962989-C-T

11705000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65962951-A-G

11705013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65962938-C-T

11705233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962719-G-A

11705293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962659-A-G

http://identifiers.org/hco/17/GRCh38#11705306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65962636-C-A

11705314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962628-A-G

11705314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962628-A-T

http://identifiers.org/hco/17/GRCh38#11705318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65962624-A-C

11705340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65962602-A-G

11705340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65962602-A-T

11705343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65962598-G-A

11705343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65962598-G-T

http://identifiers.org/hco/17/GRCh38#11705344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65962597-A-C

11705344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65962597-A-T

11705365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962579-G-T

11705393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962551-C-T

http://identifiers.org/hco/17/GRCh38#11705394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65962550-C-A

11705394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962550-C-T

11705420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962522-G-T

http://identifiers.org/hco/17/GRCh38#11705428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65962514-A-C

11705428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962514-A-G

http://identifiers.org/hco/17/GRCh38#11705445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65962503-C-A

11705448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65962500-G-T

11706340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65962156-A-G

11706462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65962035-A-G

11706602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65961893-A-G

11706743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65961676-A-G

11706789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65961627-C-T

11706818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65961585-A-G

11706897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65961521-G-A

11707654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65960223-C-T

11707954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959977-T-C

http://identifiers.org/hco/17/GRCh38#11707972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65959959-C-A

11708188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959842-T-C

11708243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959778-G-C

11708310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959714-G-A

11708931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959317-A-G

11708955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959293-G-A

11708960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959288-T-G

11708963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959285-A-G

11709057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959181-C-G

11709064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65959175-C-G

11709340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65958889-T-C

11709557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65958413-C-T

11709582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65958389-A-G

11709771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65958209-C-T

11710612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65956755-A-G

11710811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65956576-C-T

11713567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65955857-T-A

11713609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65955815-A-G

11713664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65955757-T-A

11713979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65955426-C-G

11714007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65955399-G-A

11714197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65955223-A-G

11717613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65954451-A-G

11717636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65954437-G-A

11718703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65953097-G-A

11719158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65952649-G-A

11719158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65952649-G-C

11719229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65952069-G-A

11719229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65952069-G-T

http://identifiers.org/hco/17/GRCh38#11719253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65952040-A-C

11719253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65952040-A-G

11719256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65952037-T-A

11719440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65951843-C-G

11719580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65951711-G-A

11719580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65951711-G-T

11719772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65951526-G-T

11719876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65951424-A-G

11719891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65951409-T-G

11719933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65951371-G-A

11721244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65950351-G-T

http://identifiers.org/hco/17/GRCh38#11721567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65950075-A-C

11721567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65950075-A-T

11721888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65949179-A-G

11722077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65949019-G-A

11722103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65948991-A-G

11722318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65948790-G-A

11722318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65948790-G-C

11722357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65948750-A-T

11722392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65948712-G-A

11722392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65948712-G-C

11722834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65947836-T-C

11722966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65947707-T-C

11723002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65947669-C-G

11723002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65947669-C-T

11723047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65947645-T-C

11723194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65947526-T-C

11723197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65947523-T-C

11723302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65947444-G-A

11723414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65947334-G-A

11723507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65947251-G-A

11723507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65947251-G-T

11723535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65947223-G-T

11726024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65945465-T-A

11726210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65945298-G-A

11726298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65945206-C-T

11726399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65945137-G-T

11726709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65944889-C-G

11727083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65944564-T-A

11727083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65944564-T-C

11727083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65944564-T-G

11727500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65944212-A-G

http://identifiers.org/hco/17/GRCh38#11727603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65944109-A-C

11727685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65944030-T-G

11727936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65943811-G-A

11727965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65943782-G-A

11728042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943707-T-A

11728042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943707-T-C

http://identifiers.org/hco/17/GRCh38#11728094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65943678-A-C

11728094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943678-A-G

http://identifiers.org/hco/17/GRCh38#11728126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65943651-A-C

11728126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943651-A-G

11728218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943555-G-A

http://identifiers.org/hco/17/GRCh38#11728309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65943467-C-A

http://identifiers.org/hco/17/GRCh38#11728336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65943440-A-C

11728554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943363-G-A

11728591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943327-A-T

11728708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943191-G-C

11728708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65943191-G-T

11729642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942803-T-C

11729642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942803-T-G

11729643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942802-G-T

11729677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942768-G-A

11729766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942689-A-G

11729812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942638-A-G

11729835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942617-C-G

11729835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942617-C-T

11729879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942573-A-G

11729902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942550-C-T

11729932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942513-C-T

11730256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65942225-T-C

11730402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65941984-A-T

11732015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940537-G-A

11732048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940502-G-A

11732084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940466-G-A

11732115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940435-A-G

11732115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940435-A-T

11732144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940408-T-C

11732180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940385-T-C

11732305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940275-T-C

11732323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940257-A-G

11732566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65940036-A-G

11732621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65939981-G-A

11732756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65939844-C-T

11732858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65939742-C-G

11732858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65939742-C-T

11732958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65939555-G-C

11732958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65939555-G-T

11735946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65938596-T-G

11736163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65938400-G-A

11736240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65938334-C-T

11736478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65938133-C-T

http://identifiers.org/hco/17/GRCh38#11736694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65937917-A-C

11736749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65937863-A-G

11736779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, undefined
orthologous variants: 65937834-G-T

11736798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65937815-C-T

11736995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65937617-C-T

11737152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65937459-A-T

http://identifiers.org/hco/17/GRCh38#11737215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65937399-C-A

11737215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65937399-C-T

http://identifiers.org/hco/17/GRCh38#11737409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65937210-C-A

11737448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65937171-T-C

11737480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65937140-C-T

11737524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65937093-G-A

11738728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935750-G-A

11738728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935750-G-T

http://identifiers.org/hco/17/GRCh38#11738832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65935650-C-A

11738832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935650-C-T

11738858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935624-C-T

11738958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65935529-T-C

11738958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65935529-T-G

11738973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65935514-A-G

11738973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65935514-A-T

http://identifiers.org/hco/17/GRCh38#11739084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65935408-C-A

11739086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935406-T-C

11739086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935406-T-G

http://identifiers.org/hco/17/GRCh38#11739096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65935396-C-A

11739106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935388-G-A

11739106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935388-G-C

11739106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935388-G-T

11739108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935386-G-A

11739214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65935026-C-G

11739248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65934985-C-T

11739472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65934765-C-T

11739698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65934542-T-A

11739943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65934305-G-A

11740708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65932623-G-T

11740764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65932590-T-A

11740803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65932577-A-G

11741127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65932280-T-G

11741858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65931489-A-G

11741858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65931489-A-T

11741922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65931424-C-G

11742075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65931313-G-T

11742161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65931240-C-G

11742272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65931129-A-G

11742272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65931129-A-T

11742347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65931055-C-G

11742347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65931055-C-T

11742409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65931019-G-A

http://identifiers.org/hco/17/GRCh38#11742454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65930975-C-A

http://identifiers.org/hco/17/GRCh38#11742465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65930964-C-A

11742465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65930964-C-G

11742482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65930949-T-C

http://identifiers.org/hco/17/GRCh38#11742722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65930725-C-A

11742912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65930542-T-A

11742912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65930542-T-C

http://identifiers.org/hco/17/GRCh38#11743100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65930346-C-A

11743100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65930346-C-T

11743569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65929489-C-T

11743603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65929463-C-G

11743687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65929385-G-A

11743757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65929316-G-A

11744041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65929118-G-A

11744396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928932-C-T

http://identifiers.org/hco/17/GRCh38#11744566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65928771-A-C

11744579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928760-T-C

11744673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928679-C-G

11744673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928679-C-T

11744698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928657-G-A

11744698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928657-G-T

http://identifiers.org/hco/17/GRCh38#11744741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65928625-C-A

11744741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928625-C-G

11745107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928250-G-A

11745159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65928198-A-G

11747315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65925050-C-T

11747499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65924898-T-C

11747601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65924812-G-A

11747613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65924800-G-A

11747613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65924800-G-T

11747628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65924785-T-C

11747634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65924779-G-A

11747675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: synonymous variant
orthologous variants: 65924738-G-A

11747676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65924737-C-T

11747760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65924653-A-G

http://identifiers.org/hco/17/GRCh38#11747783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65924630-C-A

11747783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65924630-C-T

http://identifiers.org/hco/17/GRCh38#11747896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65924520-A-C

11747914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65924502-G-A

11747914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65924502-G-T

11748625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65924184-T-A

11748845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65924112-C-T

11749662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65923593-C-G

11749662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65923593-C-T

11750486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65922927-C-T

11750760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65922664-A-G

11750912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65922527-T-G

11750913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65922526-A-G

11750964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65922480-T-C

11750965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65922464-A-G

http://identifiers.org/hco/17/GRCh38#11751341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65921504-A-C

11751413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65921442-A-G

11751588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65921285-T-C

http://identifiers.org/hco/17/GRCh38#11752119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65920765-A-C

http://identifiers.org/hco/17/GRCh38#11752304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65920576-C-A

11752323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920557-G-A

http://identifiers.org/hco/17/GRCh38#11752700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65920408-C-A

11752700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920408-C-G

11752719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920389-G-A

11752719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920389-G-T

http://identifiers.org/hco/17/GRCh38#11752721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65920387-A-C

11752721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920387-A-G

11752748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920369-G-A

11752773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920344-G-A

11752773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920344-G-T

11752783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920335-A-G

11752807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920311-A-G

http://identifiers.org/hco/17/GRCh38#11752998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65920088-C-A

11752998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920088-C-G

11752998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920088-C-T

11753046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920041-G-T

11753063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920024-G-A

11753063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65920024-G-T

11753103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65919986-A-G

11753103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65919986-A-T

http://identifiers.org/hco/17/GRCh38#11753112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65919977-C-A

11753112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65919977-C-T

http://identifiers.org/hco/17/GRCh38#11753287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65919812-C-A

11755714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65919411-G-A

11755714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65919411-G-C

11756547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65917937-G-A

http://identifiers.org/hco/17/GRCh38#11756712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65917780-C-A

11756731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65917761-T-C

11756731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65917761-T-G

11756744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65917749-A-G

http://identifiers.org/hco/17/GRCh38#11756792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65917621-C-A

11756792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65917621-C-G

11756792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65917621-C-T

11756793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65917620-G-A

11756979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65917432-A-G

11757341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65916300-C-T

11757348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65916293-C-T

http://identifiers.org/hco/17/GRCh38#11757395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65916252-C-A

11757395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65916252-C-G

11757395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65916252-C-T

11757436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65916216-T-C

http://identifiers.org/hco/17/GRCh38#11757454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65916198-C-A

11757515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65916137-T-G

http://identifiers.org/hco/17/GRCh38#11757635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65916017-A-C

11757652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65916000-G-A

11757652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65916000-G-C

11757728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65915928-C-T

http://identifiers.org/hco/17/GRCh38#11757764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65915887-C-A

11757864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65915800-A-T

11757959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65915705-G-A

11761367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65910015-T-C

http://identifiers.org/hco/17/GRCh38#11761379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65910000-C-A

11761379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65910000-C-G

11761379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65910000-C-T

11761444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65909878-C-T

http://identifiers.org/hco/17/GRCh38#11761571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65909758-C-A

http://identifiers.org/hco/17/GRCh38#11761780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65909553-C-A

11761979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65909396-G-A

11762012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65909363-A-G

11762031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65909344-A-G

11762031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65909344-A-T

11762347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65909029-T-C

11762406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908985-G-A

11763094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908720-G-A

11763105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908706-T-C

11763242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908578-T-C

http://identifiers.org/hco/17/GRCh38#11763349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65908471-A-C

11763349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908471-A-G

11763349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908471-A-T

http://identifiers.org/hco/17/GRCh38#11763402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65908417-C-A

11763402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908417-C-T

11763407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908412-G-A

11763407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908412-G-C

11763413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908406-C-T

11763417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908402-T-G

11763440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 65908363-G-A

11763491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: synonymous variant
orthologous variants: 65908312-T-C

http://identifiers.org/hco/17/GRCh38#11763646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65908158-C-A

11763646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908158-C-G

11763687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65908119-T-C

11763815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65907997-G-A

11763903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65907909-G-A

11764703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65907186-T-A

11764721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65907172-T-A

11764781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65907130-T-C

11764895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65907025-T-A

11765187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65906724-T-C

http://identifiers.org/hco/17/GRCh38#11765277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65906628-C-A

11765817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65905642-A-G

11765967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65905507-G-A

11765990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65905483-A-G

11766317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65905166-A-G

http://identifiers.org/hco/17/GRCh38#11767149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65904707-C-A

http://identifiers.org/hco/17/GRCh38#11767721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65897717-C-A

11767721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65897717-C-T

11767887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65897559-T-C

11767917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65897525-C-T

11767938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65897504-T-C

11768060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65897431-T-C

11768097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65897395-C-T

11768114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65897378-A-T

11768302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896806-C-T

11768314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896795-A-G

11768322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896787-G-T

11768323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896786-T-C

http://identifiers.org/hco/17/GRCh38#11768326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65896783-A-C

11768368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896738-G-A

http://identifiers.org/hco/17/GRCh38#11768369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65896737-A-C

http://identifiers.org/hco/17/GRCh38#11768371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65896735-C-A

11768371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896735-C-T

http://identifiers.org/hco/17/GRCh38#11768382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65896726-C-A

11768382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896726-C-G

11768382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896726-C-T

11768398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896710-G-A

11768418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896690-A-G

11768594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65896515-C-G

11768594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: stop gained
orthologous variants: 65896515-C-T

11768693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896432-A-G

11768697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896428-G-A

11768705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896420-T-C

11768710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896416-A-G

11768711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896415-T-C

11768870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896235-G-A

http://identifiers.org/hco/17/GRCh38#11768975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65896152-C-A

11768975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896152-C-T

11769009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896119-G-A

11769009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65896119-G-T

http://identifiers.org/hco/17/GRCh38#11769040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65896088-C-A

11769183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65895972-C-G

11769183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65895972-C-T

11769186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65895969-G-A

11769186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65895969-G-C

11769187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: synonymous variant
orthologous variants: 65895968-G-T

11769220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: synonymous variant
orthologous variants: 65895935-C-T

11769371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895786-G-A

11769371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895786-G-C

http://identifiers.org/hco/17/GRCh38#11769432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65895756-C-A

11769432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895756-C-T

http://identifiers.org/hco/17/GRCh38#11769437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65895751-C-A

11769476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895733-C-T

11769477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895732-T-C

11769563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895655-A-G

11769590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895638-C-T

11769606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895622-C-T

11769946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65895129-A-G

11774939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65890856-T-C

11774953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65890839-T-C

http://identifiers.org/hco/17/GRCh38#11775012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65890785-C-A

11775063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65890734-G-C

11775394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65890427-G-A

11775984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65890140-A-G

11776077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65890044-T-A

11776082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65890039-C-G

11776105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65890011-C-T

11776275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65889836-G-A

11776404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65889673-T-C

http://identifiers.org/hco/17/GRCh38#11776830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65889279-C-A

11777031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65889111-T-A

11777031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65889111-T-C

11777159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65888993-G-C

11777159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65888993-G-T

http://identifiers.org/hco/17/GRCh38#11777293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65888876-C-A

11777359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65888816-G-A

11777799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65888161-C-T

11779268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65885395-C-T

11779620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65885062-T-G

11779669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65885013-G-A

11779877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65884804-C-T

11780103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65884569-T-C

11780210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65884461-A-G

11780869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant
orthologous variants: 65883822-G-A

11780869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant
orthologous variants: 65883822-G-T

11780878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant
orthologous variants: 65883813-G-A

11780878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant
orthologous variants: 65883813-G-T

11780907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 65883794-A-T

11781068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65883634-A-G

11781132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65883570-A-G

11781208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65883499-G-T

http://identifiers.org/hco/17/GRCh38#11781217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65883490-C-A

11781217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65883490-C-G

http://identifiers.org/hco/17/GRCh38#11781252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65883478-C-A

11781279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65883452-G-A

11781279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65883452-G-T

11781290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65883441-G-T

11781316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65883416-T-C

http://identifiers.org/hco/17/GRCh38#11781878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65883058-A-C

11781878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65883058-A-G

11781959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65882980-A-G

11782475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65882526-T-G

11782593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65882397-A-G

11783689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: stop gained
orthologous variants: 65881316-C-T

11783815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65881181-A-G

11783815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65881181-A-T

11783854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65881146-G-A

11783854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65881146-G-T

11783939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65881072-T-C

11783984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65881027-G-A

11784198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880886-T-C

11784269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880821-T-A

11784269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880821-T-C

http://identifiers.org/hco/17/GRCh38#11784385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65880693-A-C

11784562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880523-A-T

11784579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880506-A-G

11784579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880506-A-T

11784912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880086-A-G

11784976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880037-A-G

11784976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65880037-A-T

11786020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65879724-A-G

11786061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65879684-T-G

11786125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65879645-C-T

11786260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65879515-C-T

11786281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65879111-C-G

11786297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65879095-C-T

11786751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65878396-G-C

11786783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65878361-G-T

11786819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65878314-C-T

11786978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65878154-C-T

11788043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65877897-A-G

11788173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65877768-C-T

http://identifiers.org/hco/17/GRCh38#11788205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65877736-C-A

11788280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65877656-G-A

11788814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65876980-T-A

http://identifiers.org/hco/17/GRCh38#11788831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65876963-A-C

11788882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65876915-T-A

11789432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65876422-T-A

11789554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65876235-T-C

11789997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65875841-A-G

11790236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65875610-C-G

11790295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65875543-C-T

http://identifiers.org/hco/17/GRCh38#11790421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65875389-C-A

11792327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872950-A-G

11792338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872939-A-G

11792362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872915-C-T

11792533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872765-A-G

11792631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872694-G-A

http://identifiers.org/hco/17/GRCh38#11792646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65872679-A-C

11793360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872516-T-C

11793378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872496-T-C

11793390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872484-G-C

11793390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872484-G-T

11793422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872250-A-T

11793453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65872219-A-G

11793566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65872108-C-G

11793566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65872108-C-T

11793887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65871807-C-T

11796024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65869577-T-A

11796543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65868311-C-T

11796988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867964-C-T

11797067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867862-G-A

11797115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867819-A-G

11797239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867715-G-A

11797319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867636-A-G

11797479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867482-A-G

11797479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867482-A-T

http://identifiers.org/hco/17/GRCh38#11797485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65867476-C-A

11797485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867476-C-T

11797486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867475-A-G

11797486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867475-A-T

11797490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867471-A-T

11797554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867400-G-C

11797783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65867171-A-G

11797801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65867153-T-G

http://identifiers.org/hco/17/GRCh38#11797833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65867111-C-A

11797833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65867111-C-T

11797902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65866965-G-A

11797902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65866965-G-C

11797932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65866933-T-C

11797932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65866933-T-G

11797933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65866932-G-A

11797933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65866932-G-T

11803197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864775-T-C

11803206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864766-G-A

11803312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864645-A-G

11803380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864529-G-A

11803414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864495-G-A

11803424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864485-G-T

11803629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864280-C-T

11803702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864207-A-G

11803723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864186-T-C

11803785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65864124-C-T

11804144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65863783-T-G

11804314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65863618-A-G

11804346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65863586-T-C

11804406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65863533-A-G

11804495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65863468-T-C

11806151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65862524-C-G

http://identifiers.org/hco/17/GRCh38#11806610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65861955-C-A

11806762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65861818-A-G

11806903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65861733-G-A

11806903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65861733-G-T

11807345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65861340-T-A

11807369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65861316-G-C

11807562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65861117-T-C

11807720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65860964-C-T

http://identifiers.org/hco/17/GRCh38#11807960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65858558-C-A

11807960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65858558-C-T

http://identifiers.org/hco/17/GRCh38#11808004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65858503-A-C

11808004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65858503-A-G

11808004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65858503-A-T

11808198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65858347-A-G

11808376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65858169-A-G

11808915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65857660-G-A

11809729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65856981-T-A

11809729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65856981-T-G

11809793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65856921-T-C

11809870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65856880-G-A

11809926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65856844-A-T

11810105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65856705-T-C

11810230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65856595-T-C

11810297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65856529-G-C

http://identifiers.org/hco/17/GRCh38#11812552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65856256-A-C

11813185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65855652-C-T

11813636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65855175-A-G

11815272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854963-T-C

11815293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854942-C-T

11815531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854718-G-C

11815536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854713-C-G

11816009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854559-C-T

11816173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854425-G-A

11816173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854425-G-T

11816447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854209-T-C

11816577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65854036-T-C

http://identifiers.org/hco/17/GRCh38#11816673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65853950-A-C

11817750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65852840-A-G

11818016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65852458-T-C

11818492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65852302-C-T

11818676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65852159-A-G

11818790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65852067-C-G

11818859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65851989-T-A

11818866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65851982-C-G

11819127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65851762-A-G

http://identifiers.org/hco/17/GRCh38#11819165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65851729-A-C

11821313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65847187-A-G

http://identifiers.org/hco/17/GRCh38#11821400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65847092-C-A

11821531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65846974-G-A

11821531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65846974-G-T

11821550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65846955-T-C

11821593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65846911-G-A

11821846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65846680-G-T

11822123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65846396-C-G

11822123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65846396-C-T

11822237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65846311-G-A

11822552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: synonymous variant
orthologous variants: 65846076-T-C

11822640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65845990-A-G

11822802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 65845873-C-T

http://identifiers.org/hco/17/GRCh38#11823148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65845556-C-A

11823148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65845556-C-T

http://identifiers.org/hco/17/GRCh38#11823440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65845376-C-A

11824011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844764-C-T

11824124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844639-A-G

11824139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844626-C-T

11824192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844573-T-G

11824208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844557-A-G

11824236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844490-A-G

11824385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844255-G-A

11824479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844154-C-G

11824575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65844064-T-C

11825033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65843699-C-T

11825182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65843586-T-C

11825451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65843295-A-G

11825555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65843199-G-A

11831806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65841737-T-G

11831809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65841734-C-G

11831809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65841734-C-T

11831971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65841629-G-A

11832432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65841167-C-T

11832497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65841104-A-T

11832752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840851-G-A

11832752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840851-G-T

11833021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840588-C-G

11833021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840588-C-T

11833204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840135-C-G

11833230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840114-G-A

11833267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840077-G-A

11833288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840056-A-G

11833288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65840056-A-T

11833400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65839933-T-C

11833589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65839756-G-A

http://identifiers.org/hco/17/GRCh38#11834500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65838664-C-A

11834517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65838642-T-C

11834653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65838538-G-T

11834764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65838427-G-A

11834874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: synonymous variant
orthologous variants: 65838317-G-A

11834874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense variant
orthologous variants: 65838317-G-T

11836619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65838123-C-T

11836642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65838100-T-C

11837092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65837685-A-G

11837205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65837569-G-T

11837735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833873-G-A

11837856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833751-T-C

http://identifiers.org/hco/17/GRCh38#11837886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65833728-A-C

11837890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833724-A-T

11838040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833614-G-T

11838292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833393-C-T

11838347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833341-T-A

11838380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833308-T-C

11838586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833122-G-A

http://identifiers.org/hco/17/GRCh38#11838688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65833037-A-C

11838688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833037-A-G

11838691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65833034-C-T

11838783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65832921-G-A

11838809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65832895-G-C

11838850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65832852-C-T

11838874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65832828-G-A

11842090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65830550-A-G

11842300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65830310-C-G

11842300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65830310-C-T

11843071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65829735-G-A

11843071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65829735-G-C

11843080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65829726-T-C

11843129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65829680-T-C

11843462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65829332-A-G

http://identifiers.org/hco/17/GRCh38#11843665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65829163-A-C

11844141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65828721-A-G

11844211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65828650-A-G

11848220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65826404-A-G

11848470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65826141-C-G

11849914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65822054-A-G

11850150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65821864-G-C

11850758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65821266-C-G

11850847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65821180-A-G

11850847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65821180-A-T

11850914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65821126-G-T

11850938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65821102-T-C

11851058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65820976-G-A

11851058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65820976-G-T

11851536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65820512-G-T

11851783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65820290-T-C

11853292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65819515-A-G

11853341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65819461-C-G

http://identifiers.org/hco/17/GRCh38#11853362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65819440-C-A

11853362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65819440-C-T

11853466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65819369-A-T

11853711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65819123-T-A

http://identifiers.org/hco/17/GRCh38#11853927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65818909-A-C

http://identifiers.org/hco/17/GRCh38#11854060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65818776-A-C

11854063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65818773-G-A

11854063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65818773-G-C

11854089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65818747-C-T

11854111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65818725-C-T

11854129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65818707-A-G

11854282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65818554-G-A

11854282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65818554-G-T

11854385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65818451-C-T

11856222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65816619-A-G

11856309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65816535-C-G

11856493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65816477-A-T

11858059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65815570-A-G

11858359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65815306-G-A

11867270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65811573-A-G

11867297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65811546-A-G

11867372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65811476-T-A

11867372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65811476-T-C

11867722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65810932-C-T

11867779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65810879-T-A

11867897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65810797-G-C

11868126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65810594-A-G

11868236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65810488-A-T

11868334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65810391-C-G

http://identifiers.org/hco/17/GRCh38#11868939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65809856-C-A

11869008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65809787-G-A

11869009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65809786-T-C

http://identifiers.org/hco/17/GRCh38#11869010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65809785-C-A

http://identifiers.org/hco/17/GRCh38#11869121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65809680-C-A

11869121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65809680-C-T

11869123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65809678-T-A

11869151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65809650-G-A

http://identifiers.org/hco/17/GRCh38#11869336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65809480-C-A

11869336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65809480-C-T

11869404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65809399-G-A

11869503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65809301-A-G

11869641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65809204-G-A

11869721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65809125-C-T

11869760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65809086-C-T

11870285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65808019-C-T

11870566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65807008-T-C

11870643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65806932-G-A

11871153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65806514-C-T

http://identifiers.org/hco/17/GRCh38#11871179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65806487-A-C

11871183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65806483-A-G

11871265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 65806402-G-A

11871398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65806262-C-T

http://identifiers.org/hco/17/GRCh38#11871500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65806143-C-A

11871500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65806143-C-G

http://identifiers.org/hco/17/GRCh38#11871519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65806125-C-A

11871519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65806125-C-T

11871620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65806026-A-G

11871683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant
orthologous variants: 65805963-T-C

http://identifiers.org/hco/17/GRCh38#11871849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65805811-C-A

11871849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65805811-C-T

11871850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65805810-G-A

11871850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65805810-G-T

11871880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65805780-T-C

http://identifiers.org/hco/17/GRCh38#11871897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65805767-C-A

11871897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65805767-C-T

http://identifiers.org/hco/17/GRCh38#11871911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65805753-C-A

11871911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65805753-C-G

11871911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65805753-C-T

11873191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65805326-G-T

11873482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804076-T-C

11873569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803991-G-T

11873782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803772-T-G

11873872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803674-G-A

11874184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803521-G-T

http://identifiers.org/hco/17/GRCh38#11874242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65803486-C-A

11874242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803486-C-T

11874513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803373-G-T

11874876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65802912-A-G

11874989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65802810-T-A

http://identifiers.org/hco/17/GRCh38#11875045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65802754-C-A

11875045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65802754-C-T

http://identifiers.org/hco/17/GRCh38#11875074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65802725-C-A

11875074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65802725-C-T

11875257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65802542-T-A

11875257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65802542-T-C

11875266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65802533-T-A

11875266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65802533-T-C

11880016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65797841-A-G

11880037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65797820-G-T

11880038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65797819-C-T

http://identifiers.org/hco/17/GRCh38#11880051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65797806-C-A

11880085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 65797779-C-T

http://identifiers.org/hco/17/GRCh38#11880154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65797710-C-A

http://identifiers.org/hco/17/GRCh38#11880328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65797541-C-A

11880328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65797541-C-T

11880885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796537-T-G

11881070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796365-A-T

http://identifiers.org/hco/17/GRCh38#11881106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65796326-C-A

11881106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796326-C-T

http://identifiers.org/hco/17/GRCh38#11881273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65796161-A-C

11881273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 65796161-A-T

11881330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65796104-T-C

11881420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65795998-A-G

http://identifiers.org/hco/17/GRCh38#11881469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65795950-C-A

11881469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65795950-C-T

11881531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65795892-T-A

11881531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65795892-T-C

11881551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65795872-A-G

11881572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65795851-A-G

11881815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65795798-G-A

11882083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65795639-G-T

11882221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65795493-G-A

11882670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65795035-C-T

11882686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65795019-A-G

11882763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65794839-A-T

http://identifiers.org/hco/17/GRCh38#11882788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65794816-C-A

11882788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron variant
orthologous variants: 65794816-C-T

11883433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786991-T-C

11883497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786928-G-A

http://identifiers.org/hco/17/GRCh38#11883528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65786883-C-A

http://identifiers.org/hco/17/GRCh38#11883535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65786877-C-A

http://identifiers.org/hco/17/GRCh38#11883619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65786796-A-C

11883619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65786796-A-T

11883653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65786762-C-G

11883653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65786762-C-T

11883655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65786760-C-T

11883700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65786715-G-A

11883700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65786715-G-C

11883700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65786715-G-T

11883743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65786672-A-G

11883757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65786659-C-T

http://identifiers.org/hco/17/GRCh38#11883803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65786619-C-A

11883804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786618-A-G

11883822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786594-A-G

11884161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786136-G-A

11884186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786108-T-A

11884197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786097-A-G

11884202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786092-T-A

11884202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786092-T-C

11884206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786088-T-A

11884206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786088-T-C

11884206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786088-T-G

http://identifiers.org/hco/17/GRCh38#11884242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65786055-C-A

11884284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786025-T-C

11884609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785713-T-A

11884706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785608-T-G

11884756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785562-G-C

http://identifiers.org/hco/17/GRCh38#11886448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65777900-C-A

11886616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777759-C-T

11886687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777685-A-G

11886779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777615-G-T

http://identifiers.org/hco/17/GRCh38#11886796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65777598-C-A

11886796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777598-C-G

11886796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777598-C-T

11887022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777382-A-G

11887046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777358-C-G

11887046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777358-C-T

11887324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777084-G-C

11887324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777084-G-T

http://identifiers.org/hco/17/GRCh38#11887861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65776542-A-C

11889830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775050-C-T

11889873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775000-C-T

http://identifiers.org/hco/17/GRCh38#11890578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65774386-A-C

http://identifiers.org/hco/17/GRCh38#11891709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65772671-C-A

11891709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65772671-C-T

11891891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65772508-A-G

http://identifiers.org/hco/17/GRCh38#11891893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65772506-C-A

11891893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65772506-C-T

11891962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65772437-A-T

11891964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65772435-G-A

11891964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65772435-G-T

11892197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65772219-T-A

11892555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65771978-C-T

11893325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65771623-G-A

11893325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65771623-G-T

11894439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65771042-G-A

11894456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65771025-C-T

11894465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65771016-T-A

11894503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65770978-A-G

11894567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770930-G-A

11894567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770930-G-T

11894619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770877-A-G

11894619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770877-A-T

11894987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770494-C-T

11895011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770467-C-T

11895161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770341-A-G

11895324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770191-C-G

11895324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770191-C-T

11895330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770185-G-A

11895339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770176-C-T

11897566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65770015-T-A

11897741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769774-G-A

11897741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769774-G-T

11897887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769653-G-A

11898439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769458-G-A

11898647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769246-T-C

11898722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769175-T-A

11898841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769069-G-A

11898855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769055-C-T

11898863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769047-T-G

11898876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65769034-G-A

11898966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65768948-A-T

11899020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65768861-A-T

11899987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65767910-C-T

11900188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65767731-G-A

11900197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65767722-T-A

11900496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65767469-C-G

11900496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65767469-C-T

11900680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65767316-G-T

11900800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65767167-G-A

11900800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65767167-G-T

11902240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765577-G-A

11902240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765577-G-T

11902301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765550-T-C

11902633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765237-G-T

http://identifiers.org/hco/17/GRCh38#11902648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65765216-C-A

11902648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765216-C-G

http://identifiers.org/hco/17/GRCh38#11902653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65765212-C-A

11902653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765212-C-T

http://identifiers.org/hco/17/GRCh38#11902654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65765211-C-A

11902671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765194-G-A

11902671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765194-G-C

11902671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65765194-G-T

11902916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65764943-G-T

11902948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65764915-A-G

11902956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65764907-A-G

11902986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65764877-G-T

11902987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65764876-G-T

11903000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65764863-G-A

11903000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65764863-G-T

11903009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65764854-A-G

11903353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65763419-T-A

11903479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65763263-T-C

11903500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65763243-C-T

11903591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65763158-G-A

11903603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65763146-G-A

11905292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65762228-G-A

11905479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65762063-A-G

http://identifiers.org/hco/17/GRCh38#11905535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65762011-C-A

11905535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65762011-C-G

11905535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65762011-C-T

11905810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 65761743-G-A

11905903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65761652-T-G

http://identifiers.org/hco/17/GRCh38#11905959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65761591-C-A

11905959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65761591-C-T

11914592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65758024-A-G

11915207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65757547-T-C

11916263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65756736-T-A

11916379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65756633-T-C

11916543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65756489-C-T

11916666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65756371-C-T

http://identifiers.org/hco/17/GRCh38#11916797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65756250-A-C

11917417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65755855-A-G

11917904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65755413-A-G

11917959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65755358-G-A

11917959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65755358-G-C

11918121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65755197-C-T

11919536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65754836-G-A

11919586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65754787-T-G

11920652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65753327-G-A

11920656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65753323-G-A

11921000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65753070-T-A

11921000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65753070-T-G

11921190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65752972-G-T

11921431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65752779-G-T

11921465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65752753-C-T

11921525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65752695-G-C

11921620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65752592-C-T

11921743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65752468-A-G

11922598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65751628-T-A

11922654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65751584-C-T

11922894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65751370-A-G

11922913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65751352-A-T

11923170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65751037-G-A

11923232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750955-C-T

11923295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750875-T-C

11923296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750874-T-C

11923299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750871-A-T

11923671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750489-A-G

11923671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750489-A-T

http://identifiers.org/hco/17/GRCh38#11923712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65750454-C-A

11923712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750454-C-G

11923712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750454-C-T

11923801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750371-A-G

11923801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750371-A-T

11923999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750164-T-A

11923999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750164-T-C

http://identifiers.org/hco/17/GRCh38#11924091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65750089-C-A

11924091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65750089-C-T

11924344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65749839-G-A

11924548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65749696-T-C

11924663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65749579-G-A

11924710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65749538-G-A

http://identifiers.org/hco/17/GRCh38#11925541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65748978-C-A

11925541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65748978-C-G

http://identifiers.org/hco/17/GRCh38#11925552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65748969-C-A

11925552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65748969-C-G

11925552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65748969-C-T

11925569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65748952-A-G

11925709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65748797-G-T

11927607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65748206-T-C

11927743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65748077-C-T

11927883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65747949-A-G

11928331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65747701-G-A

http://identifiers.org/hco/17/GRCh38#11928506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65747532-C-A

11928713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65747339-G-C

11928713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65747339-G-T

11928924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65747172-A-G

11929729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65746372-T-A

11929729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65746372-T-G

11929796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65746306-G-A

11929796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65746306-G-T

11929995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65746109-A-G

11929995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65746109-A-T

11930008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65746096-T-C

11930100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65746004-C-T

11930122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65745982-G-A

11930164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65745939-G-A

11930164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65745939-G-C

11930164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65745939-G-T

11930941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65745386-C-G

http://identifiers.org/hco/17/GRCh38#11931138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65744702-A-C

11931402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65744477-G-A

http://identifiers.org/hco/17/GRCh38#11931476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65744409-C-A

11931476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65744409-C-T

http://identifiers.org/hco/17/GRCh38#11931726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65742338-C-A

11931872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742194-G-A

11931872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742194-G-T

11931874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742192-T-C

11931887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742143-T-C

11931927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742103-A-G

11931961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742069-C-T

11931971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742060-G-A

11931971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742060-G-T

11932071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65741962-T-C

11932137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65741896-C-T

11932179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65741854-T-C

11932284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741816-G-A

11932284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741816-G-T

11932286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741814-G-A

11932301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741807-T-C

http://identifiers.org/hco/17/GRCh38#11932770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65741631-A-C

11932781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741620-C-G

11932781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741620-C-T

11932782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741619-G-A

11932806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741595-T-C

11932942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741452-C-G

11932968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741422-G-A

11932973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741417-C-T

http://identifiers.org/hco/17/GRCh38#11933000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65741303-C-A

11933000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741303-C-G

11933731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740992-T-C

11933731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740992-T-G

11933838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740923-A-G

11933986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65740785-T-C

http://identifiers.org/hco/17/GRCh38#11934161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65740615-C-A

11934161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740615-C-T

11934182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740601-G-A

http://identifiers.org/hco/17/GRCh38#11934205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65740582-A-C

11934205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740582-A-G

11934284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740507-G-T

11935738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740130-T-A

11935738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740130-T-C

11935739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65740129-A-G

11936146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739764-T-C

http://identifiers.org/hco/17/GRCh38#11937334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65739268-C-A

11937334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739268-C-G

11937335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739267-T-C

11937335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739267-T-G

11937415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65739188-A-G

http://identifiers.org/hco/17/GRCh38#11937433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65739170-A-C

11937567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739047-A-G

11937601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739016-A-G

http://identifiers.org/hco/17/GRCh38#11937618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65739000-C-A

11937618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739000-C-T

http://identifiers.org/hco/17/GRCh38#11937674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65738959-C-A

11937674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738959-C-G

11937674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738959-C-T

11937705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738926-A-T

11937746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738884-G-C

11937773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738861-C-T

11937945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738689-T-C

11937948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738686-G-A

11938126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738538-C-T

11938141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738528-T-C

http://identifiers.org/hco/17/GRCh38#11938532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65738438-C-A

11938532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738438-C-G

11939777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65735374-G-C

11940152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65735035-G-A

11940187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65735001-T-G

11940342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734863-C-T

11940392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734814-T-A

11940541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734665-C-T

11940599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734592-T-G

11940685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734506-A-G

11940803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734388-G-A

11940803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734388-G-C

11941305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733925-G-A

11941311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733919-C-T

11941374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733859-C-T

11941487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733746-G-A

11941588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733657-G-A

11941842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733307-A-G

11941963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733167-C-T

http://identifiers.org/hco/17/GRCh38#11942236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65732938-C-A

11942236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65732938-C-T

http://identifiers.org/hco/17/GRCh38#11942278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65732273-C-A

11942278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65732273-C-G

11942278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65732273-C-T

11942297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65732254-G-A

11942297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65732254-G-C

11942357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65732194-C-G

11942357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65732194-C-T

11942372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 65732179-A-T

11942521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65732047-G-T

11942589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731976-T-A

11942589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731976-T-C

11942598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731967-A-G

11942602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731963-T-C

11943766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731465-T-C

11944187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731032-A-G

11944762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65730569-T-C

11944943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65730439-A-G

11945039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730360-G-A

11945176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730278-T-A

11948583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729236-T-C

11949017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728633-C-T

11949294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728357-T-C

11949447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728217-T-C

11949496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728150-T-A

11949515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728127-C-T

11949710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727934-A-G

11949912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727613-A-T

11949961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727567-A-G

11949961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727567-A-T

11950692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726794-T-C

11951042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726457-C-T

http://identifiers.org/hco/17/GRCh38#11961720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65725412-C-A

11961720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65725412-C-T

11961785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65725389-T-C

11961785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65725389-T-G

11961916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65725263-A-T

11962011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65725168-G-A

11962061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65725118-G-A

11962061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65725118-G-C

11962116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65725063-C-T

11968194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723735-T-C

11968216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723718-T-G

11968276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723661-A-G

http://identifiers.org/hco/17/GRCh38#11968292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65723647-C-A

11968571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723423-T-A

11968574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723419-T-G

11968879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723127-A-G

http://identifiers.org/hco/17/GRCh38#11969148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#65722726-C-A

11969164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722706-A-G

11969239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722667-A-T

11969561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65722349-T-C

11969563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65722347-G-A

11969563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65722347-G-T

11969570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65722340-A-G

11969646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65722275-T-A

11969646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65722275-T-C

11969674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65722247-A-G

11969674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2953
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65722247-A-T