191199327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27126471-T-C

191199481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27126638-A-T

191199592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27126790-T-C

191199742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27126946-T-G

191199762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27126959-T-C

191199767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27126964-T-G

191199920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27127102-A-G

http://identifiers.org/hco/3/GRCh38#191200431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27127673-C-A

191200431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27127673-C-T

191200484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27127730-T-C

191200559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27127786-T-G

http://identifiers.org/hco/3/GRCh38#191200827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27128042-C-A

191200827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27128042-C-T

191200941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27128150-C-T

http://identifiers.org/hco/3/GRCh38#191201234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27128476-C-A

191201234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27128476-C-T

191201421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27128722-T-C

191201588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27129361-T-C

191201651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27129427-T-C

191201817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27129693-A-G

191202062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27130069-T-C

191202137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27130142-A-G

191202163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27130167-G-T

191202212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27130218-G-T

191202478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27133614-T-C

191202492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27133628-A-T

191202752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27133852-G-A

191203011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27134111-T-G

191203015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27134115-T-C

191203043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27134136-G-T

191203065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27134158-A-T

191203255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27134351-C-T

191203322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27134418-A-G

191203329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27134428-C-T

http://identifiers.org/hco/3/GRCh38#191203570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27134641-A-C

191206849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27135321-C-T

191206879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27135373-A-G

191206958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27135451-G-A

191206958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27135451-G-T

191206988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27135481-T-C

191207101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27135593-G-A

191207105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27135597-C-T

191207311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27135816-T-C

191207655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27136073-A-T

191207757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27136142-G-C

191207878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27136220-T-C

191208017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27136439-T-A

191208033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27136455-C-T

191208074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27136487-C-T

191208408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27136949-G-T

191208637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27137178-A-G

http://identifiers.org/hco/3/GRCh38#191208694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27137234-C-A

191208694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27137234-C-G

191211146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27138660-A-G

191211286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27138928-C-G

191211291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27138933-C-T

191211557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27139195-A-G

http://identifiers.org/hco/3/GRCh38#191211584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27139224-A-C

191211592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27139232-C-T

http://identifiers.org/hco/3/GRCh38#191211692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27139334-A-C

191211824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27139430-G-A

191211903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27139509-T-C

191212051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27139653-A-G

http://identifiers.org/hco/3/GRCh38#191212307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27139880-A-C

191212625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: synonymous variant
orthologous variants: 27140181-A-G

http://identifiers.org/hco/3/GRCh38#191212645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27140198-C-A

191212645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27140198-C-G

191212645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27140198-C-T

http://identifiers.org/hco/3/GRCh38#191213393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27140716-C-A

191213404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27140727-T-A

191213404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27140727-T-C

191213466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27140776-G-T

191213477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27140787-T-C

http://identifiers.org/hco/3/GRCh38#191213494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27140810-A-C

http://identifiers.org/hco/3/GRCh38#191217518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27142401-A-C

191217599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27142481-T-G

191217678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27142560-A-G

191217678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27142560-A-T

191218257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143083-C-T

191218370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143144-A-G

191218633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143214-G-A

191218633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143214-G-T

http://identifiers.org/hco/3/GRCh38#191218712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27143238-C-A

191218712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143238-C-T

191218779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 27143299-A-T

191218819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: missense_variant, undefined
orthologous variants: 27143339-A-G

191218821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: synonymous_variant, undefined
orthologous variants: 27143341-A-G

191218830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: synonymous_variant, undefined
orthologous variants: 27143350-C-G

191218866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: synonymous_variant, undefined
orthologous variants: 27143386-T-C

191218866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: missense_variant, undefined
orthologous variants: 27143386-T-G

191218965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143485-A-T

191218992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143508-T-C

191219047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143603-A-G

191219312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143958-G-A

191219312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27143958-G-C

191219489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144156-T-C

191219549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144215-G-A

191219568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144234-C-T

191219590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144268-G-T

191219709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144407-C-G

191219796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144445-G-A

http://identifiers.org/hco/3/GRCh38#191219807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27144487-A-C

191219807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144487-A-G

191219931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144593-T-A

191219931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144593-T-C

191220023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144689-T-C

191220175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144817-T-A

191220194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27144834-A-G

http://identifiers.org/hco/3/GRCh38#191228686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27148080-C-A

191228823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27148221-G-A

191228994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27148392-T-C

191229029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27148454-C-T

191229035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27148460-A-G

191229281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27148683-A-G

http://identifiers.org/hco/3/GRCh38#191229320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27148719-A-C

191229357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27148756-T-C

http://identifiers.org/hco/3/GRCh38#191229359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27148784-A-C

191229436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27148937-T-A

191230979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150046-G-A

191231125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150394-C-T

191231206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150473-G-A

191231206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150473-G-T

191232985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150661-C-G

191232985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150661-C-T

191233122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150785-A-G

191233155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150818-C-T

191233170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150830-A-G

191233196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150841-A-G

191233246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27150891-C-T

191233434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27151081-G-A

http://identifiers.org/hco/3/GRCh38#191234767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27151522-C-A

http://identifiers.org/hco/3/GRCh38#191234775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27151530-A-C

191234804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27151566-T-C

191234846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27151608-C-G

http://identifiers.org/hco/3/GRCh38#191234951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27151713-C-A

191235002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27151767-C-G

191235075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27151826-C-T

http://identifiers.org/hco/3/GRCh38#191235092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27151843-A-C

191235142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27151890-A-G

191235151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27151897-T-C

191235194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27151938-T-C

191235199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27151943-G-A

191235353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27152091-G-A

191235597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27152315-C-T

191235656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27152374-C-T

191235693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27152411-G-A

191235887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27152574-A-G

191235976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27152636-T-A

191236191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27152839-A-G

191236194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27152842-C-T

191237263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153119-C-T

191237287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153143-G-A

191238001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153282-A-G

191238037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153317-G-A

http://identifiers.org/hco/3/GRCh38#191238084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27153365-A-C

http://identifiers.org/hco/3/GRCh38#191238165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27153444-C-A

191238165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153444-C-G

191238165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153444-C-T

191238744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153552-T-C

191238848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153634-G-C

191239058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27153778-C-T

191239551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27154111-G-A

191239906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27154429-G-A

191239906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27154429-G-T

http://identifiers.org/hco/3/GRCh38#191240957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27155929-A-C

191240957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27155929-A-G

191244388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27162746-G-A

http://identifiers.org/hco/3/GRCh38#191244436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27162792-A-C

191244436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27162792-A-G

191244713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163012-C-T

191244760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163053-A-G

191244765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163058-G-T

191244882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163174-A-G

http://identifiers.org/hco/3/GRCh38#191245073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27163261-C-A

191245330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163406-A-G

191245350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163426-C-T

191245361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163437-G-T

191245431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163507-G-C

191245540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163615-G-A

191245641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163709-G-A

191245657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27163725-T-C

191249820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165458-G-C

191249920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165505-T-A

191249920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165505-T-C

191249961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165546-A-T

http://identifiers.org/hco/3/GRCh38#191249999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27165584-C-A

191249999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165584-C-T

http://identifiers.org/hco/3/GRCh38#191250157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27165741-C-A

191250157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165741-C-T

191250177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165759-T-C

191250230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165812-T-G

191250257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165843-T-C

191250258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27165844-T-C

http://identifiers.org/hco/3/GRCh38#191251362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27166769-A-C

191251379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27166800-G-A

191251379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27166800-G-T

191251426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27166862-C-T

191251501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27166898-A-G

191252441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167488-A-G

191252537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167575-T-C

191252611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167636-C-T

191252612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167637-G-A

191252612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167637-G-T

191252625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167652-T-G

191252646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167673-G-A

191252881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167834-A-G

191252904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27167857-A-G

191253090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168021-G-A

191253257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27168247-G-A

191253295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron_variant, undefined
orthologous variants: 27168284-C-T

191261697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168363-T-C

191261725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168389-T-C

191261731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168395-G-T

http://identifiers.org/hco/3/GRCh38#191261758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27168419-C-A

191261765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168426-A-G

191261804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168463-T-C

191261804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168463-T-G

191262252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168596-A-G

191262398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168737-G-C

191262565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168885-A-G

191262614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27168928-T-C

191262747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27169042-G-A

191262747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27169042-G-T

191262750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27169045-T-G

191262804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27169095-G-T

191262851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: intron variant
orthologous variants: 27169143-C-T

http://identifiers.org/hco/3/GRCh38#191262869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27169161-C-A

191262870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 27169162-A-G

191262956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169236-C-T

http://identifiers.org/hco/3/GRCh38#191262964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27169244-C-A

http://identifiers.org/hco/3/GRCh38#191262967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27169247-C-A

191262967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169247-C-T

http://identifiers.org/hco/3/GRCh38#191262996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27169278-C-A

191262998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169280-A-G

191262998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169280-A-T

191263025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169307-A-G

191263055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169337-G-A

191263072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169353-A-G

191263099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169380-C-T

191263105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169386-C-G

191263106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169387-T-A

191263106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169387-T-G

191264546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169677-T-C

191264547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169678-T-C

191264648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169777-G-A

191264648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29961
most severe consequence: 3 prime UTR variant
orthologous variants: 27169777-G-T