34151326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548505-G-A

http://identifiers.org/hco/11/GRCh38#34151367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103548476-C-A

http://identifiers.org/hco/11/GRCh38#34151395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103548471-C-A

34151395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548471-C-T

34151550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548339-C-T

34151552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548337-G-A

34151607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548290-A-G

34151736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548204-G-A

34151736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548204-G-T

http://identifiers.org/hco/11/GRCh38#34151749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103548191-A-C

34151749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548191-A-G

http://identifiers.org/hco/11/GRCh38#34151831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103548165-C-A

34151831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548165-C-T

34151853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548138-T-C

34151853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548138-T-G

34151879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548119-C-T

34151886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548112-T-C

34151950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548060-G-A

34151950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548060-G-T

34151987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103548020-A-G

34152010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103547998-T-G

34152279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103547811-G-A

34152279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103547811-G-C

34152361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103547737-G-A

34152361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 3 prime UTR variant
orthologous variants: 103547737-G-T

34152496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103547591-T-G

34152574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103547513-G-T

http://identifiers.org/hco/11/GRCh38#34152663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103547434-C-A

34152663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103547434-C-T

34152870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103547211-A-G

34152958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103547145-T-C

34154094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546653-A-T

34154124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546625-T-C

34154135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546614-C-T

34154154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546600-A-G

34154218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546537-G-A

34154218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546537-G-T

34154237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546521-G-T

http://identifiers.org/hco/11/GRCh38#34154299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103546462-A-C

http://identifiers.org/hco/11/GRCh38#34154493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103546128-C-A

34154493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103546128-C-T

http://identifiers.org/hco/11/GRCh38#34154502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103546119-C-A

34154503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546118-T-A

34154503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546118-T-C

34154514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546107-G-A

34154514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103546107-G-T

34154681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103545922-C-G

34154681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103545922-C-T

http://identifiers.org/hco/11/GRCh38#34154684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103545919-C-A

34154684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103545919-C-G

34154684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103545919-C-T

34154788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103545827-C-G

34154813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103545804-G-A

http://identifiers.org/hco/11/GRCh38#34154889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103545734-C-A

34154949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103545671-C-T

34155656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103544949-A-G

34157400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103544449-C-G

http://identifiers.org/hco/11/GRCh38#34157466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103544402-C-A

34157466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103544402-C-T

34157502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103544397-C-T

34157561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103544348-G-A

http://identifiers.org/hco/11/GRCh38#34157692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103544263-C-A

34158048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103544036-A-G

34158054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103544030-A-G

34159146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542962-G-A

34159146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542962-G-T

34159159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542946-G-A

34159159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542946-G-C

34159159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542946-G-T

34159199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542899-G-T

34159223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542884-C-T

34159425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542693-T-C

34159554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542572-G-A

34159695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542424-C-T

34159836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103542071-G-C

34160041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541761-T-G

34160199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541633-A-G

34160204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541628-G-A

34160232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541614-G-A

34160232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541614-G-T

34160349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103541495-T-C

34160427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541421-T-C

34160503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541405-C-G

34160503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541405-C-T

34160723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541269-G-A

34160723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541269-G-C

34160734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541258-T-A

34160734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541258-T-G

34160743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541250-T-G

34160893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541207-C-T

34160919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103541181-A-G

http://identifiers.org/hco/11/GRCh38#34161092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103541011-C-A

34161092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103541011-C-T

http://identifiers.org/hco/11/GRCh38#34161149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103540970-C-A

34161149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103540970-C-G

http://identifiers.org/hco/11/GRCh38#34161653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103540675-A-C

34161653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103540675-A-G

34162262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103540022-G-A

34162262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103540022-G-T

34162641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103539784-T-C

34162846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103539578-C-T

34162847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103539577-A-T

34162854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103539570-G-A

34162854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103539570-G-T

34162986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103539492-C-T

34163110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103539394-C-T

34164107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103539114-A-T

34164331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538913-A-G

34164332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538912-A-G

34164485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538768-A-T

http://identifiers.org/hco/11/GRCh38#34164588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103538653-C-A

34164588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538653-C-T

34164613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538631-G-A

http://identifiers.org/hco/11/GRCh38#34164629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103538615-C-A

34164629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538615-C-T

34164647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538597-G-A

34164647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538597-G-T

34164701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103538543-G-A

34164701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103538543-G-C

34164701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103538543-G-T

34164740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103538504-G-A

34164749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103538495-C-T

34164785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103538459-C-T

34164794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103538450-A-G

http://identifiers.org/hco/11/GRCh38#34164914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103538344-C-A

34164915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538343-T-C

34164932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538326-G-T

http://identifiers.org/hco/11/GRCh38#34165047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103538215-C-A

34165050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538212-C-T

34165094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103538168-G-T

http://identifiers.org/hco/11/GRCh38#34165189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103538071-C-A

34165277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103537999-T-A

34165292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103537984-G-A

34165292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103537984-G-C

34165292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103537984-G-T

http://identifiers.org/hco/11/GRCh38#34165325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103537951-C-A

34165325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103537951-C-T

http://identifiers.org/hco/11/GRCh38#34165369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103537911-C-A

34165369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537911-C-G

34165369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537911-C-T

http://identifiers.org/hco/11/GRCh38#34165389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103537892-C-A

34165389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537892-C-T

34165415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537868-G-T

http://identifiers.org/hco/11/GRCh38#34165497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103537786-C-A

34165497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537786-C-T

34165541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537744-T-C

34165552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537733-A-G

http://identifiers.org/hco/11/GRCh38#34165663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103537628-C-A

34165776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537390-C-G

34165782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537384-G-A

34165802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537321-C-T

34165858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103537227-C-T

34165947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537134-A-G

34165973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537113-C-T

34166131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103537059-G-A

34166289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103536919-T-A

34166617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103536581-G-T

34166708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103536523-C-T

34166814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103536411-C-T

34166933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103536308-A-G

34167082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103536206-T-C

34167332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103536002-G-T

http://identifiers.org/hco/11/GRCh38#34167441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103535871-A-C

34167441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103535871-A-T

34167671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103535674-C-T

34167791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103535578-G-T

34167970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103535418-G-A

34168019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103535371-A-G

http://identifiers.org/hco/11/GRCh38#34168045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103535346-A-C

34168045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103535346-A-G

34168047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103535344-G-A

34168047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103535344-G-T

34168062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103535328-T-C

34168568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103534964-C-G

34168682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103534856-G-A

34168947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103534617-G-A

34169064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103534500-C-T

34169244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103534291-C-T

34169531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103534061-T-C

34169670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103533933-C-T

34169737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103533876-A-G

34169755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103533860-C-T

34170792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532881-G-A

34170792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532881-G-T

http://identifiers.org/hco/11/GRCh38#34170836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103532828-C-A

34170836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532828-C-T

34171093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532577-G-A

34171093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532577-G-C

34171093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532577-G-T

34171158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532550-T-C

34171219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532508-G-A

34171219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532508-G-C

34171219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532508-G-T

34171677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103532218-G-T

34171891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531998-G-A

http://identifiers.org/hco/11/GRCh38#34171901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103531991-A-C

34172517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531805-C-T

34172933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531475-A-G

34172933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531475-A-T

34173015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531405-G-A

34173015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531405-G-C

34173015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531405-G-T

34173023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531399-T-C

http://identifiers.org/hco/11/GRCh38#34173064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103531361-C-A

34173074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531351-A-T

http://identifiers.org/hco/11/GRCh38#34173086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103531339-A-C

34173113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103531312-A-G

http://identifiers.org/hco/11/GRCh38#34173308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103531113-C-A

34173314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103531107-G-A

34173314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103531107-G-T

http://identifiers.org/hco/11/GRCh38#34173361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103531065-C-A

34173361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103531065-C-T

34176729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103530230-T-G

34178039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103528973-C-T

34178634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103528447-C-G

34178665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103528410-G-A

34179589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103527278-C-T

34179916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103526958-G-A

34180031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103526840-T-C

34180105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103526774-T-C

34181352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103526240-C-T

34181386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103526206-C-T

34181565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103526037-G-A

34181850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525773-G-A

34181850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525773-G-T

34182031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525613-G-A

34182387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525260-A-G

34182438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525206-C-G

34182471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525174-T-C

34182473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525172-C-G

http://identifiers.org/hco/11/GRCh38#34182496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103525150-C-A

34182496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525150-C-G

34182496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525150-C-T

34182507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525139-G-A

34182507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525139-G-C

34182507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525139-G-T

34182514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525134-T-A

34182514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525134-T-C

34182531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525117-A-G

34182568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525080-T-C

34182644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103524607-C-T

34182928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103524376-A-G

34184141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103523118-T-G

34184464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103522846-G-A

34184584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103522747-C-T

34186271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103521432-G-A

34186271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103521432-G-T

34186633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103521071-T-C

34187091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103520622-G-A

http://identifiers.org/hco/11/GRCh38#34187096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103520617-A-C

34187978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103519885-C-T

34188234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103519667-C-T

34188287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103519619-C-T

34188501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103519417-C-G

34188607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103519317-T-C

34189033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518929-A-G

34189044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518918-G-T

http://identifiers.org/hco/11/GRCh38#34189160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103518815-C-A

34192418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518307-G-A

34192429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518296-G-A

34192579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518171-G-T

34192693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518070-C-T

34192705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518058-C-T

34193053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103517821-C-G

34193141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103517733-G-A

34193545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103517360-G-A

34193915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516995-C-G

34193976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516933-G-T

http://identifiers.org/hco/11/GRCh38#34194722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103516305-C-A

34194722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516305-C-T

34194821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516219-C-T

34195052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515986-C-T

34195168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515914-G-A

34195369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515708-A-G

34195386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515691-C-T

34195409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515664-T-A

34195586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515501-G-A

34196616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103514455-T-C

34196782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103514371-G-C

34196917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103514250-G-A

34197145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513978-C-T

http://identifiers.org/hco/11/GRCh38#34197176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103513953-A-C

34197176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513953-A-G

http://identifiers.org/hco/11/GRCh38#34197433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103513726-C-A

34197433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 103513726-C-T

http://identifiers.org/hco/11/GRCh38#34197499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103513660-C-A

34197499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103513660-C-T

34197572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513613-G-A

34197572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513613-G-C

34197572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513613-G-T

34197599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513590-T-C

http://identifiers.org/hco/11/GRCh38#34197613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103513576-C-A

34197613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513576-C-G

34197613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513576-C-T

34197648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513552-T-G

http://identifiers.org/hco/11/GRCh38#34197677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103513525-C-A

34197711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513491-C-T

34197782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513408-C-T

http://identifiers.org/hco/11/GRCh38#34197911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103513308-C-A

34198755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512935-G-A

34198821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512868-G-A

34198840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512849-A-G

34198865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512787-G-A

34199332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512326-C-T

34199445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512217-A-G

34199476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512187-G-C

34199505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512160-A-G

34199735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103512016-T-C

34199819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103511940-C-T

34199993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103511775-C-T

34200913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103510821-G-C

http://identifiers.org/hco/11/GRCh38#34201240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103510212-C-A

34201240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103510212-C-T

34201380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103510070-C-T

34201392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103510058-A-G

34201415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103510035-C-T

34201445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103510008-T-G

34201597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509859-A-G

34201597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509859-A-T

34201709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509747-G-T

34202023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509511-C-T

34202135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509405-A-T

34202143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509400-C-T

34204600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103509178-A-G

34204693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103509085-A-G

http://identifiers.org/hco/11/GRCh38#34204747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103509036-C-A

34204747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509036-C-T

http://identifiers.org/hco/11/GRCh38#34204753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103509026-C-A

34204753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509026-C-T

http://identifiers.org/hco/11/GRCh38#34204757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103509022-C-A

34204757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509022-C-T

34204794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508990-C-T

34204818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508973-T-C

34204869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508924-G-A

34204869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508924-G-C

http://identifiers.org/hco/11/GRCh38#34204949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103508863-A-C

34205346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103508534-C-G

34205549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508371-A-G

34205734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508201-C-T

34206722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507804-C-T

34206863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507689-T-C

34207006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507581-C-T

34207313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507292-A-G

34207407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507200-T-C

34207426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507181-A-G

34207450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507157-T-C

34207506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507101-T-G

34207536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507071-A-G

34210183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505350-T-G

34210330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505245-A-T

34210405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505165-T-C

34210421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505149-A-G

34210451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505057-C-T

34210758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504828-A-T

34210788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504798-G-A

34210999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504431-C-T

34211451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504310-G-A

34211536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504224-A-G

34213862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103502679-T-C

34213867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103502674-T-A

34213968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103502576-T-A

34214146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103502421-A-G

34215351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500799-C-T

http://identifiers.org/hco/11/GRCh38#34215503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103500661-C-A

34215503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500661-C-T

34215625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500562-G-A

34216007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500242-T-C

34222786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499092-G-C

34223281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103498647-G-A

34225169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103495182-T-C

34226424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103494303-G-A

34230208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493457-C-G

34230208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493457-C-T

34230532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493211-C-T

34230564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493180-G-C

34230614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493124-C-T

34234147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103492763-C-T

34234196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103492708-G-C

34234202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103492702-G-A

34234420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103492446-C-T

34234756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103492144-C-T

34235225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103492027-T-C

34235450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103491833-T-C

http://identifiers.org/hco/11/GRCh38#34235766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103491575-A-C

34236555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103490757-G-A

34236624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103490699-T-C

34239909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103489468-G-C

34240045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103489395-T-C

34240229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103489074-C-T

34240348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103488990-A-T

34240379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103488960-A-G

34240503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103488856-C-T

34241848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103488618-A-G

http://identifiers.org/hco/11/GRCh38#34241866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103488600-C-A

34241935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103488532-G-C

34242254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103488238-C-T

34242454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103488024-G-A

34242454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103488024-G-T

34242466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103488005-A-G

34242517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103487959-C-G

34242517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103487959-C-T

34242519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103487957-G-C

34242519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103487957-G-T

34242560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103487919-G-A

34242560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103487919-G-C

34242560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103487919-G-T

34242576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103487903-G-T

http://identifiers.org/hco/11/GRCh38#34242640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103487858-C-A

34242658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103487840-G-T

34242662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103487787-A-G

34242690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103487768-G-T

34242693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103487763-G-A

34242693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103487763-G-T

34243009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103487517-C-T

34243437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103486957-T-C

34243473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103486921-C-T

http://identifiers.org/hco/11/GRCh38#34243558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103486835-A-C

34243806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103486605-C-G

34243806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103486605-C-T

34243807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103486604-G-A

34243807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103486604-G-C

34244082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103486360-G-C

34244376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103486083-C-G

34244400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103486061-C-G

34244591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103485906-G-C

34244613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103485883-C-T

34244661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103485844-G-A

34244669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103485836-T-C

http://identifiers.org/hco/11/GRCh38#34245557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103485360-C-A

34245557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103485360-C-G

34245557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103485360-C-T

34245721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103485224-C-G

34246003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103484986-G-A

34246018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103484971-C-T

34248608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103482741-A-T

34248651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103482691-C-T

34250017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103481916-G-C

34250081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103481855-G-T

34250721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103481797-G-C

34250724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103481794-C-T

34250809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103481709-G-T

34250906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103481625-C-T

34251099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103481464-C-G

34251245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103481338-G-A

34251281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103481309-T-C

34251344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103481257-G-T

34251566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103481043-C-T

34251651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103480936-C-T

34251787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103480806-C-T

34251880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103480707-C-T

http://identifiers.org/hco/11/GRCh38#34252095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103480520-A-C

34254919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103480185-A-G

34254947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103480158-G-A

34254972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103480137-T-C

34255008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103480102-G-T

34255982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103479583-C-T

34256062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103479508-T-C

34256145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103479454-G-A

34256427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103479196-A-G

34256488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103479137-G-A

34256531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103479094-C-T

34256775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103478667-C-T

34256790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103478652-C-T

34256889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103478401-T-C

34257137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103478156-T-C

34257279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103478046-C-T

34257367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103477975-G-A

34257957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103477309-T-C

34258097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103477204-C-T

http://identifiers.org/hco/11/GRCh38#34258478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103476877-A-C

http://identifiers.org/hco/11/GRCh38#34258553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103476800-A-C

34260218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103476461-C-T

34260297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103476388-G-A

34260537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103476180-C-T

34260604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103476110-A-G

34260673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103476037-G-A

34261237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103475737-A-G

34261237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103475737-A-T

34261706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103475141-T-A

34262528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103474386-C-G

34263094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103473819-G-A

34263241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103473701-A-T

34263655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103472313-G-A

34263665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103472305-T-C

34263676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103472294-G-C

34264127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103471969-T-C

34264328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103471773-A-G

34264626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103471483-C-T

34264736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103471405-G-A

34264736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103471405-G-C

34264739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103471402-C-T

34264855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103471302-C-G

34264855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103471302-C-T

http://identifiers.org/hco/11/GRCh38#34265019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103471147-A-C

34265054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103471113-G-A

34266868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103470144-G-T

34267139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103469926-C-T

34267224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103469843-G-A

34267779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103469047-T-C

34268996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103468639-T-C

34269578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103468162-A-G

34269607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103468133-G-T

34269678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103468069-A-G

34269712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103468035-C-T

34271924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103465976-G-A

34272691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103465706-A-T

34272759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103465661-G-A

34272759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103465661-G-T

34273145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103465352-A-G

34273537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103464953-C-T

http://identifiers.org/hco/11/GRCh38#34273568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103464887-C-A

34273568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103464887-C-T

34273599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103464856-T-C

34273695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103464772-A-G

34274442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103464343-C-T

34274562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103464226-C-T

34274583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103464172-G-A

34274603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103464122-T-A

34274653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103464075-A-G

34274811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103463827-T-A

34274811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103463827-T-C

34275208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103463417-A-G

34275254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103463371-C-T

34275308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103463319-A-G

34275372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103463257-A-G

34275373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103463256-T-G

34275462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103463177-C-T

34275790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103462871-T-C

34276032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103462653-A-G

34276269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103462239-C-T

34276456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103462061-T-C

34278240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103461025-C-G

34278306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103460949-T-C

34278639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103460674-G-A

34278688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103460661-C-T

34278799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103460609-C-T

34279033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103460392-A-G

34279049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103460376-T-C

34279075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103460348-A-G

34279160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103460264-G-A

http://identifiers.org/hco/11/GRCh38#34279227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103460185-A-C

34280223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103459949-G-C

34280275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103459896-G-A

34281634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103459305-C-T

34281706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103459233-G-T

34281741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103459200-A-T

34281742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103459199-T-C

34281877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103459017-A-T

34281911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103458990-G-A

34281933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103458968-A-T

34282176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103458741-C-T

34283587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103457406-A-G

34283647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103457354-T-C

34283748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103457243-T-G

34283989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103457015-A-G

34284109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103456895-A-G

34284305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103456680-G-A

34284510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103456474-C-T

34284521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103456463-C-T

http://identifiers.org/hco/11/GRCh38#34284770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103456282-C-A

34284830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103456219-T-C

34285404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103455651-G-A

34285562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103455491-C-G

http://identifiers.org/hco/11/GRCh38#34285565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103455488-A-C

34285661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103455413-T-C

34285699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103455352-G-A

34285830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103455223-T-C

34285842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103455211-G-A

34285994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103455068-G-C

34286647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103454988-C-T

http://identifiers.org/hco/11/GRCh38#34286698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103454937-A-C

34286744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103454891-C-G

34286867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103454778-A-T

34287020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103454630-G-A

34287926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103454051-T-A

34287926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103454051-T-C

34287927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103454050-C-T

34287935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103454042-C-T

34288064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103453915-A-G

34288349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103453735-G-A

34288633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103453488-G-A

34288697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103453424-C-G

34288763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103453362-G-A

34290228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103449860-A-G

34290775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103449305-A-T

34290983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103449099-C-G

34291090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103448990-G-A

34291370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103448743-G-C

34291407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103448705-T-C

34291499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103448635-T-G

34291510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103448624-T-G

34291885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103448523-T-G

34291908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103448501-T-G

34295301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103445572-G-A

34295485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103445406-T-A

34295734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103445168-C-T

34296243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103444871-C-T

34296497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103444636-G-A

34296757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103444397-T-G

34297388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103443762-A-G

34297397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103443754-C-T

34297436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103443715-T-C

34298089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103443469-T-G

34298463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103443199-T-A

34298525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103443167-T-C

http://identifiers.org/hco/11/GRCh38#34298952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103442941-C-A

34299168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442726-G-T

34299302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442584-G-A

http://identifiers.org/hco/11/GRCh38#34299338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103442549-A-C

34299358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442516-T-A

34299359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442515-T-A

34299360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442514-A-T

34299454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442426-G-A

34299490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442389-T-A

34299490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442389-T-C

34299567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442316-G-A

34299611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442273-A-G

http://identifiers.org/hco/11/GRCh38#34299813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103442068-C-A

34299839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442042-G-A

34299840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103442041-C-T

34300243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103441673-G-T

34300978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103440840-C-T

34301085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103440791-C-T

34301311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103440604-T-A

34301389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103440526-C-T

34301392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103440523-G-A

http://identifiers.org/hco/11/GRCh38#34301506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103440398-A-C

34302226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103440313-T-C

34302615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103439960-C-T

34302754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103439834-G-C

34302915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103439713-G-A

34303014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103439616-T-C

34303358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103439325-G-T

http://identifiers.org/hco/11/GRCh38#34303408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103439275-A-C

34304771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103438965-G-A

34304774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103438962-G-A

34304997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103438757-T-C

34305022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103438724-T-G

34305284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103438461-C-G

34305476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103438275-A-G

34306057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103437679-A-G

34306766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103437418-G-C

34306960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103437223-G-A

34306972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103437211-T-A

http://identifiers.org/hco/11/GRCh38#34306973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103437210-C-A

34306982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103437201-T-A

34307548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103436665-C-T

34307574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103436636-G-A

34308089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103436226-G-A

34308110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103436205-G-A

34308275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103436070-T-C

34308943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103435729-A-G

34310092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103434407-G-A

34310114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103434384-C-T

34311017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103433848-C-T

34311082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103433811-C-T

34311130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103433782-C-T

34311297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103433642-T-C

34311459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103433474-T-C

http://identifiers.org/hco/11/GRCh38#34311714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103433271-C-A

34311724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103433261-G-A

34312353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103432953-C-T

34312536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103432730-A-G

http://identifiers.org/hco/11/GRCh38#34312956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103432425-C-A

34313263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103432154-C-T

http://identifiers.org/hco/11/GRCh38#34313441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103431983-C-A

34313441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103431983-C-T

34313595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103431929-A-G

http://identifiers.org/hco/11/GRCh38#34314969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103430964-A-C

34315369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103430559-C-T

http://identifiers.org/hco/11/GRCh38#34315604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103430356-C-A

34315604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103430356-C-T

34315786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103430186-C-T

34316130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103429843-G-A

34316822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103429131-C-G

34317161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103428831-A-G

34317161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103428831-A-T

34319039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103427876-T-C

34319369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103427582-C-T

34319420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103427538-G-A

34319420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103427538-G-T

34320448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103427165-A-G

34324705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103425521-A-G

34325245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103425151-T-C

34325358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103425057-G-T

34325502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103424905-A-G

34325502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103424905-A-T

34326303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103424502-T-C

34326308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103424497-G-A

34327078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103424139-A-G

34327466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103423766-G-A

34327878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103423174-C-G

34327878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103423174-C-T

34328030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103423022-A-G

34328348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103422668-G-A

34328523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103422494-A-T

34328538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103422479-C-T

34329465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103421266-T-C

34329477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103421254-A-G

34329477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103421254-A-T

34329582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103421149-C-T

34329940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103420824-A-G

34329965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103420802-C-T

34330095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103420679-A-G

34330234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103420585-G-A

34330312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103420506-T-G

34330961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103419818-A-T

34331129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103419658-G-A

34331231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103419574-C-T

34331540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103419244-G-A

34331707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103419078-C-T

34332410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418443-G-A

34332422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418431-C-T

34332542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418304-T-A

34332651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418228-C-G

34332683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418197-G-A

34332683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418197-G-T

34332711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418169-G-C

34332869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418015-G-A

34332875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103418009-G-A

34332950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103417968-C-T

34332951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103417967-G-A

34333007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103417916-A-G

34333029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103417894-C-T

34333222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103417697-G-T

34336956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103415794-C-T

34337230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103415561-C-T

34337497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103415206-A-G

34337915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103414713-C-T

34339621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103413766-T-C

34339971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103413432-G-C

34340302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103413201-G-A

34340302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103413201-G-T

34340965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103412554-C-G

34340989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103412530-T-C

34341129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103412394-A-T

34341783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103411780-A-G

34341872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103411698-A-T

34342751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103410867-T-C

34343146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103410718-C-T

34343718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103410423-C-T

34343864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103410323-T-C

34343872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103410315-C-G

34343917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103410288-T-C

34344453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103409841-T-C

34344454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103409840-A-G

34345035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103409493-C-G

34345040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103409488-G-A

34345040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103409488-G-T

34345114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103409425-C-T

34345154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103409386-G-T

34345197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103409357-T-C

34345236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103409318-G-A

34345236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103409318-G-T

http://identifiers.org/hco/11/GRCh38#34345536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103409074-C-A

34345698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103408928-C-T

34345700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103408926-T-A

34345989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103408675-C-T

http://identifiers.org/hco/11/GRCh38#34346054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103408617-A-C

http://identifiers.org/hco/11/GRCh38#34346055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103408616-C-A

34346148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103408522-G-A

http://identifiers.org/hco/11/GRCh38#34346510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103408173-A-C

34347149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103407525-C-T

34347875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103407151-A-G

34348001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103407023-A-T

34348157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103406911-T-G

http://identifiers.org/hco/11/GRCh38#34348730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103406368-A-C

34348997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103405884-C-G

34349039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103405841-T-C

34349108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103405775-T-A

34349138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron_variant, undefined
orthologous variants: 103405570-G-A

34349210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103405502-A-G

http://identifiers.org/hco/11/GRCh38#34349425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103405299-C-A

http://identifiers.org/hco/11/GRCh38#34349690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103405050-C-A

34349690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103405050-C-T

34350039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103404693-A-G

34350163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103404570-C-T

34350359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103404144-C-T

34350374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103404129-C-T

34350467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103404031-C-T

34350693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103403895-A-T

34350708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103403880-C-T

34350839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103403738-G-C

34351417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103403529-G-C

34351611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103403332-T-C

34351905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103403030-G-T

http://identifiers.org/hco/11/GRCh38#34351959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103402964-C-A

34351959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103402964-C-T

34352235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103402693-T-C

http://identifiers.org/hco/11/GRCh38#34352411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103402526-A-C

34352411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103402526-A-T

34353120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103401853-C-T

34353162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103401833-A-G

34353247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103401719-T-C

http://identifiers.org/hco/11/GRCh38#34353270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103401689-C-A

34353830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103401150-G-C

34353917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103401062-C-G

34354301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103400742-G-A

34354301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103400742-G-C

34354301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103400742-G-T

http://identifiers.org/hco/11/GRCh38#34354467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103400688-A-C

34354467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103400688-A-G

34354543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103400683-A-G

34355688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398925-C-T

34355880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398745-C-T

34356195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398404-A-G

34356218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398381-C-T

34356246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398353-T-A

34356246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398353-T-C

34356258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398340-G-A

34356325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398275-T-C

34356362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398238-G-A

34356368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103398232-G-A

34356666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: intron variant
orthologous variants: 103397974-T-C

34356727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, undefined
orthologous variants: 103397926-T-G

34356802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, undefined
orthologous variants: 103397851-T-C

34356802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, undefined
orthologous variants: 103397851-T-G

http://identifiers.org/hco/11/GRCh38#34356982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103397671-C-A

34356982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103397671-C-T

34357492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, undefined
orthologous variants: 103397161-C-T

34357528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, undefined
orthologous variants: 103397125-G-A

34357528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense_variant, undefined
orthologous variants: 103397125-G-T

34357570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: missense variant
orthologous variants: 103397083-T-G

34357680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396967-G-A

34357680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396967-G-T

34357764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396883-G-A

34357764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396883-G-T

http://identifiers.org/hco/11/GRCh38#34357810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103396837-C-A

34357810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396837-C-T

34357812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396835-G-A

34357812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396835-G-T

http://identifiers.org/hco/11/GRCh38#34357822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103396824-C-A

34357970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396693-T-C

34357970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5 prime UTR variant
orthologous variants: 103396693-T-G

34358009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23842
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103396654-G-A