94437012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118245759-C-T

94437086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118245822-G-A

94437086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118245822-G-T

94437178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118245881-T-A

94437382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246107-C-T

94437482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246203-T-A

94437483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246204-G-A

94437759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246487-T-A

94437987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246710-A-G

94438005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246728-G-A

94438035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246758-G-A

94438072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246801-T-C

94438105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246834-T-C

94438202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246930-C-T

94438249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246976-T-C

94438252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118246979-A-G

94438288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247012-A-G

94438327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247056-G-A

94438327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247056-G-T

94438337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247066-A-G

94438351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247080-G-C

94438351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247080-G-T

94438409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247142-T-C

http://identifiers.org/hco/13/GRCh38#94438429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118247153-A-C

94438429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247153-A-G

94438429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247153-A-T

94438441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247165-G-C

94438441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247165-G-T

94438449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247173-T-C

94438449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247173-T-G

94438474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247198-A-G

94438503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247236-G-A

94438515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247248-T-A

94438515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118247248-T-G

94438702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248083-C-G

94438702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248083-C-T

http://identifiers.org/hco/13/GRCh38#94438732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118248120-C-A

94438739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248127-T-C

94438739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248127-T-G

94438813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248201-G-T

94438837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248225-C-T

94438951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248305-T-C

94438957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248311-G-A

94438957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248311-G-T

http://identifiers.org/hco/13/GRCh38#94438963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118248317-C-A

94439074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248416-G-A

94439074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248416-G-T

http://identifiers.org/hco/13/GRCh38#94439106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118248435-C-A

94439148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248478-T-G

94439197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248519-T-C

94439206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248528-G-A

http://identifiers.org/hco/13/GRCh38#94439255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118248577-A-C

http://identifiers.org/hco/13/GRCh38#94439284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118248606-C-A

94439291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248613-G-T

94439322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248645-G-T

http://identifiers.org/hco/13/GRCh38#94439358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118248673-C-A

94439358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248673-C-T

94439387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3 prime UTR variant
orthologous variants: 118248701-G-T

94439622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250207-T-A

94439622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250207-T-G

94439677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250257-G-T

94439680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250260-G-A

94439680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250260-G-T

94439681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250261-G-T

94439754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250328-T-C

94439755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250329-T-C

http://identifiers.org/hco/13/GRCh38#94439756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118250330-C-A

94439766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250341-T-G

94439798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250373-A-T

94439804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250379-A-T

94439815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250396-G-T

94439864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250427-G-T

94439866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 118250429-C-T

http://identifiers.org/hco/13/GRCh38#94439888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118250433-C-A

http://identifiers.org/hco/13/GRCh38#94439896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118250441-C-A

94439907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 118250452-T-C

94439928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 118250473-T-C

94439962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118250507-C-T

94440070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118250615-A-G

94440155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118250690-T-A

94440155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118250690-T-G

http://identifiers.org/hco/13/GRCh38#94440402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118250933-C-A

94440420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118250951-G-A

94440464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118250995-A-T

94442962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118255577-C-T

94442982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118255598-A-G

94442999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118255612-T-G

94443292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118255869-T-C

94443306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118255883-G-A

94443306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118255883-G-T

94443324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118255901-G-T

http://identifiers.org/hco/13/GRCh38#94443367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118255943-A-C

94443367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118255943-A-G

94443584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 118256152-A-G

94443719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256265-G-A

94443719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256265-G-T

94443738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256282-A-G

94443754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256298-A-G

94443754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256298-A-T

94443874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256351-G-A

94443879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256356-A-G

94443901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256378-G-T

94443978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256453-G-T

94444033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256507-G-C

94444374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118256645-T-C

94444374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118256645-T-G

94444380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118256650-C-T

94444414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118256689-C-T

94444428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 118256702-A-G

94444443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 118256717-A-G

94444443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 118256717-A-T

http://identifiers.org/hco/13/GRCh38#94444494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118256768-C-A

94444530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256807-T-C

94444564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256841-A-G

94444626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256909-C-G

94444638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256921-T-A

94444705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118256983-G-T

94446163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118257431-G-A

94446285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118257541-T-A

94446310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118257566-A-G

94446387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118257643-C-G

94446437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118257690-G-A

94446498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118257747-T-C

http://identifiers.org/hco/13/GRCh38#94446537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118257809-A-C

94446657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118257911-G-A

94446865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118258046-T-A

94447657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118259298-T-C

94448502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118259810-T-C

94448949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118259921-G-A

94448951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118259923-C-T

94449127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260089-G-A

94449223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260178-G-T

94449285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260216-G-A

94449381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260314-T-C

http://identifiers.org/hco/13/GRCh38#94449416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118260345-A-C

94449529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260434-G-C

94449643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260554-G-A

94449714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260743-A-G

94449786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260829-T-C

94449885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118260927-C-T

94450011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118261028-A-G

94450150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118261196-G-A

http://identifiers.org/hco/13/GRCh38#94450176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118261223-C-A

94450664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262232-C-G

94450664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262232-C-T

94450671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262239-A-G

94450738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262313-G-C

94450962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262539-C-T

94451128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262670-T-A

94451145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262687-T-G

94451202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262744-A-T

94451310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262847-G-T

94451377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118262901-T-A

94451648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118263104-A-G

94451794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118263330-A-G

94451804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118263345-G-A

94451818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118263359-G-A

94451925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118263473-T-G

94451995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118263538-A-G

94452013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118263556-A-T

94452769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118264609-G-A

94452799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118264634-T-C

94452811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118264644-T-A

94452811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118264644-T-C

94452827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118264662-G-A

http://identifiers.org/hco/13/GRCh38#94452924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118264752-A-C

94454393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118267197-T-C

94455021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118267851-G-A

94455078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118267915-A-G

http://identifiers.org/hco/13/GRCh38#94455186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118267967-C-A

94455315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268068-G-C

94455319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268072-C-T

94455367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268106-G-C

94455381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268112-T-G

94455439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268147-T-C

94455454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268162-T-A

94455590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268406-C-T

94455592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268408-G-C

94455592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268408-G-T

94455956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268807-G-A

94455956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268807-G-T

94456061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118268894-A-G

94457427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118269809-A-G

94457850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118270164-A-G

94458029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118270335-T-C

94458110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118270389-G-A

94458201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118270464-T-C

94458304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118270564-T-C

94459786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118271311-C-T

94459847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118271413-A-G

http://identifiers.org/hco/13/GRCh38#94459868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118271434-C-A

94460196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 118271755-A-G

94460196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118271755-A-T

94460330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118271873-G-T

94460341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118271884-A-G

94460353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118271893-G-A

94460353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118271893-G-T

http://identifiers.org/hco/13/GRCh38#94460354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118271894-C-A

94461540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273246-T-G

94461554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273260-G-A

94461701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273396-A-G

94461707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273402-C-T

http://identifiers.org/hco/13/GRCh38#94461824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118273502-A-C

94461824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273502-A-G

94461824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273502-A-T

94461829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273507-T-C

http://identifiers.org/hco/13/GRCh38#94461879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118273552-C-A

94461879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273552-C-G

94461879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273552-C-T

http://identifiers.org/hco/13/GRCh38#94461912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118273585-A-C

94461976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273781-T-G

94461981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118273786-G-T

94462081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 118273934-G-A

94462220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118274070-T-C

94462232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118274082-G-A

94462232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118274082-G-T

94462248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118274098-C-T

94462884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118274393-A-G

94463763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118275060-G-A

94463850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118275123-T-A

94464050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118275342-C-T

94464887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118276387-C-G

94464985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118276485-C-T

94465123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118276627-C-T

94465254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118276744-A-G

94465445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118276856-T-G

94465527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118276939-G-A

94465600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118276999-T-C

94465609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118277009-C-T

94465630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118277019-T-G

94465794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118277183-G-T

94465821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277210-A-G

94465821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277210-A-T

94465866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277255-G-A

94465866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277255-G-T

94465894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277283-T-C

94465910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277299-G-C

94465910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277299-G-T

94465975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277353-T-C

94466087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277495-A-G

94466196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277591-G-T

94466209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277604-G-C

94466328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277684-T-C

94466352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277708-G-C

94466417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277766-T-C

94466417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277766-T-G

http://identifiers.org/hco/13/GRCh38#94466444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118277787-C-A

94466513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277840-A-T

94466519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118277846-T-A

94466584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118277899-A-G

94466670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118277985-G-C

94466670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118277985-G-T

94466685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118277995-G-A

94466685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118277995-G-T

94466726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278034-G-T

http://identifiers.org/hco/13/GRCh38#94466742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118278048-C-A

94466742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278048-C-G

94466742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278048-C-T

94466842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278138-A-G

http://identifiers.org/hco/13/GRCh38#94466958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118278274-C-A

94466958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278274-C-T

94466960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278276-A-G

http://identifiers.org/hco/13/GRCh38#94466978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118278294-A-C

http://identifiers.org/hco/13/GRCh38#94466991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118278305-A-C

94466991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278305-A-G

http://identifiers.org/hco/13/GRCh38#94467051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118278361-C-A

94467051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278361-C-T

http://identifiers.org/hco/13/GRCh38#94467071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118278382-A-C

94467071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278382-A-G

94467100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278411-A-G

94467155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278467-G-A

94467225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278538-G-T

http://identifiers.org/hco/13/GRCh38#94467244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118278557-C-A

94467244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278557-C-T

94467318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278631-G-T

94467319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278632-T-C

94467420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278732-G-C

http://identifiers.org/hco/13/GRCh38#94467451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118278763-C-A

94467566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118278866-C-T

94467706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118279016-C-T

http://identifiers.org/hco/13/GRCh38#94467820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118279343-C-A

http://identifiers.org/hco/13/GRCh38#94467828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118279350-C-A

http://identifiers.org/hco/13/GRCh38#94467839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118279361-C-A

94467839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118279361-C-T

http://identifiers.org/hco/13/GRCh38#94467865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118279387-C-A

http://identifiers.org/hco/13/GRCh38#94467868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118279390-C-A

94467999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118279509-G-A

94468042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118279551-T-G

94468043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118279552-T-C

94468126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118279630-A-G

94468291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118279986-T-A

http://identifiers.org/hco/13/GRCh38#94468295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118279990-C-A

94468295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118279990-C-T

94468307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280002-G-A

94468307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280002-G-C

94468351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280046-A-G

94468379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280073-A-G

http://identifiers.org/hco/13/GRCh38#94468386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118280080-C-A

http://identifiers.org/hco/13/GRCh38#94468415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118280105-A-C

94468415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280105-A-G

http://identifiers.org/hco/13/GRCh38#94468446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118280136-C-A

94468446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280136-C-T

94468493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280177-G-A

94468493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280177-G-T

http://identifiers.org/hco/13/GRCh38#94468580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118280254-C-A

94468609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280283-T-C

94468621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280287-A-G

94468632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280303-G-T

http://identifiers.org/hco/13/GRCh38#94468651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118280325-C-A

94468651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118280325-C-G

94468873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118280547-G-A

94468873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 118280547-G-T

94468946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118280620-G-A

94468946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118280620-G-C

94468960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118280634-C-G

94468983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118280657-G-A

94468983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118280657-G-T

94469056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280730-A-G

94469074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280749-G-T

94469132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280807-G-A

94469132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280807-G-T

94469140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280833-G-T

94469170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280902-G-T

94469528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281239-G-A

94469553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281257-C-T

94469617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281318-G-T

94469796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281456-T-G

94469802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281462-C-T

94469813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281472-G-A

94469813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281472-G-T

94469847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281514-G-A

94469872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281532-C-T

94469886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281546-C-G

94470194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281690-T-C

94470197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281693-C-T

94470296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281787-A-G

http://identifiers.org/hco/13/GRCh38#94470528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118282001-A-C

94470699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282156-T-C

94471787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282598-T-G

94473920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284981-C-T

94473948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285009-G-A

94474114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285148-C-T

94474357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285376-G-A

94474840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285855-A-G

94475128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286113-A-T

94475189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286170-C-T

94475268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286250-T-G

94475627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286709-T-C

http://identifiers.org/hco/13/GRCh38#94475834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118286995-A-C

94475834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286995-A-G

http://identifiers.org/hco/13/GRCh38#94475907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118287059-A-C

94475994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287153-A-G

94476249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287363-A-T

http://identifiers.org/hco/13/GRCh38#94476793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118287614-A-C

94476927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287751-T-C

94477840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288085-G-A

94478002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288243-T-C

94478108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288339-A-T

94478551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288494-T-C

94478681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288618-C-G

94478734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288671-C-T

94478749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288686-A-G

94478788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288722-G-C

94478911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288827-T-C

94478942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118288855-C-T

94479084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118289019-G-A

94479084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118289019-G-C

94479110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118289045-G-A

94479175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118289110-T-G

http://identifiers.org/hco/13/GRCh38#94479332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118289263-C-A

94479332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118289263-C-T

http://identifiers.org/hco/13/GRCh38#94479376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118289333-C-A

94479450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118289423-G-A

94479450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118289423-G-T

94479451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118289424-C-T

94479733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118289708-G-A

94479733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118289708-G-T

94479743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118289720-G-A

94479752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118289744-T-A

94479790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118289782-T-C

94479929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118289922-G-A

94480078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118290070-A-G

94480078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118290070-A-T

94480224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118290218-C-G

94480230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118290224-A-G

94480299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118290279-T-C

http://identifiers.org/hco/13/GRCh38#94480427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118290413-A-C

94480471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118290448-T-C

http://identifiers.org/hco/13/GRCh38#94480575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118290548-A-C

94480575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118290548-A-G

94480974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118291051-A-G

94481083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118291161-A-G

94481151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2709
most severe consequence: intron variant
orthologous variants: 118291211-C-T