http://identifiers.org/hco/7/GRCh38#107765565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31523784-C-A

107765703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31523646-T-C

107765929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31523423-A-G

107765929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31523423-A-T

107765936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31523416-T-A

107765936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31523416-T-C

107766395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31522453-G-A

107766445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31522403-G-A

107766461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31522393-G-A

107766605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31522288-A-G

107766605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31522288-A-T

107766615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31522278-C-G

107766923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31521970-A-T

107767134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31521785-C-T

107767455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31521503-A-T

107767997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31520759-G-A

107767997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31520759-G-T

107768015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31520741-G-A

107768015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31520741-G-T

107768040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31520720-T-A

107768121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31520682-G-T

107768835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31519979-G-A

107768857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31519957-T-C

107768868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31519946-C-T

http://identifiers.org/hco/7/GRCh38#107768954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31519903-A-C

http://identifiers.org/hco/7/GRCh38#107771715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31519073-C-A

107771796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31519003-G-T

107771856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518940-A-G

107771904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518895-T-G

107771928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518869-G-A

107771928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518869-G-T

107772002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518799-C-T

107772019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518782-T-C

107772124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518502-G-A

107772124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518502-G-C

107772124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518502-G-T

107772127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518499-T-C

107772185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518450-T-C

107772185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518450-T-G

107772248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518396-G-T

107772275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518369-C-T

107772293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518348-C-T

107772382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31518272-T-C

107772519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31517951-A-G

107772641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31517838-T-C

107773295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31517140-A-G

http://identifiers.org/hco/7/GRCh38#107773408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31517040-C-A

107774016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 31516531-G-A

107774026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31516521-T-C

107774027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31516520-C-T

107774053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31516494-A-T

107774062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31516485-G-A

107774062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31516485-G-T

107774128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31516419-G-A

107774128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31516419-G-C

107774128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31516419-G-T

107774169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31516374-A-G

107774202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31516338-G-T

http://identifiers.org/hco/7/GRCh38#107774743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31515879-C-A

107774743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31515879-C-T

107774796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31515832-C-G

107774796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31515832-C-T

107774820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31515808-T-C

107775950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31515370-A-G

107775970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31515349-A-T

107776006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31515313-G-A

107776006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31515313-G-T

107776057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515282-T-A

107776068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515271-T-C

http://identifiers.org/hco/7/GRCh38#107776109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31515231-C-A

107776109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515231-C-T

http://identifiers.org/hco/7/GRCh38#107776158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31515194-C-A

107776158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515194-C-G

107776243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515111-T-C

107776243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515111-T-G

http://identifiers.org/hco/7/GRCh38#107776253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31515101-A-C

107776271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515083-A-G

107776291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515064-G-T

107776309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31515046-G-A

107776387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31514973-A-G

107776596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31514783-T-C

107776613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31514766-A-G

107776615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31514764-G-A

107776736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31514633-T-C

107776743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31514628-A-T

107776744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31514627-T-C

107776775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514605-T-A

107776796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514580-G-A

107776796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514580-G-T

107776816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514561-A-G

107776942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514443-C-T

107777000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514385-G-T

107777071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514315-G-A

107777071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514315-G-C

107777709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31514248-G-T

http://identifiers.org/hco/7/GRCh38#107778027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31513808-C-A

107778027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31513808-C-T

107778064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31513685-A-T

107778160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31513585-A-T

107778181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31513564-G-C

http://identifiers.org/hco/7/GRCh38#107778202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31513543-A-C

107778202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31513543-A-G

http://identifiers.org/hco/7/GRCh38#107778208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31513537-A-C

107778211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31513534-G-A

107778313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31513431-T-A

107778313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31513431-T-C

107778480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31513323-G-A

107778703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31513134-A-G

107779072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31512934-A-G

http://identifiers.org/hco/7/GRCh38#107779395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31512597-A-C

107779395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31512597-A-G

http://identifiers.org/hco/7/GRCh38#107779541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31511927-A-C

107779541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31511927-A-G

107779555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31511913-A-G

http://identifiers.org/hco/7/GRCh38#107779588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31511881-A-C

107779588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31511881-A-G

http://identifiers.org/hco/7/GRCh38#107779594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31511875-A-C

http://identifiers.org/hco/7/GRCh38#107779611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31511858-A-C

107779636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31511833-T-C

107779747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31511721-A-G

107779833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31511638-G-C

107779833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31511638-G-T

http://identifiers.org/hco/7/GRCh38#107779864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#31511611-C-A

107779868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31511607-G-A

107779868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31511607-G-T

http://identifiers.org/hco/7/GRCh38#107779906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#31511570-C-A

107779906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31511570-C-T

http://identifiers.org/hco/7/GRCh38#107779954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#31511529-A-C

107780084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31511411-T-C

107780686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31510697-C-T

107780926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31510136-G-A

107781041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31510043-G-C

107781213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31509935-T-C

107781269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31509893-C-G

107781285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31509877-T-G

107781678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31509244-A-T

107781731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31509190-G-C

107781867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31509057-G-C

107782395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31508610-G-A

107782667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31507666-G-T

107782786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31507543-G-C

107782786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31507543-G-T

107782867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31507464-C-T

107782875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 31507456-C-T

107782972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31507359-T-A

107782972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31507359-T-G

107783115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31507217-A-G

107783125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31507207-G-A

107783125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31507207-G-T

http://identifiers.org/hco/7/GRCh38#107783182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31507157-C-A

107783281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31507066-A-T

107783290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31507057-C-T

http://identifiers.org/hco/7/GRCh38#107783324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#31507023-C-A

107783324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31507023-C-G

107783324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31507023-C-T

107783436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506912-C-T

107783489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506846-T-C

107783516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506819-C-T

107783626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506714-C-T

107783648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506692-C-T

107783717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506624-A-G

http://identifiers.org/hco/7/GRCh38#107783726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31506615-C-A

107783768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506566-A-G

107783825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506524-C-G

107783970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506379-C-T

http://identifiers.org/hco/7/GRCh38#107784048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31506317-A-C

107784262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31506099-A-T

107784351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31505992-A-G

http://identifiers.org/hco/7/GRCh38#107784378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31505970-A-C

107784378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31505970-A-G

107785181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31505513-A-G

107785840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31504799-T-C

107785851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31504788-C-G

107786055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31504623-T-G

107786106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31504574-G-A

107786533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31504161-G-C

107786546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31504140-T-C

107786773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31503998-A-G

107786774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31503997-C-T

107786801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31503970-G-T

107786811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31503960-T-A

107786816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31503955-G-T

107786954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31503818-T-A

107787020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31502967-C-G

107787043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31502944-T-A

107787104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31502891-T-C

http://identifiers.org/hco/7/GRCh38#107787205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31502786-C-A

107787342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31502659-A-G

107787388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31502614-A-T

107787475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31502527-G-A

107787477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31502525-C-T

107787541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31502462-C-T

http://identifiers.org/hco/7/GRCh38#107787812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31502148-A-C

107787812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31502148-A-G

107787814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31502146-T-C

107787946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31501955-G-T

107789512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31500988-A-G

107789548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31500952-G-C

107789597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31500903-A-G

http://identifiers.org/hco/7/GRCh38#107789794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31500719-C-A

107789794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31500719-C-G

http://identifiers.org/hco/7/GRCh38#107789827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31500695-C-A

107790194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31500178-G-A

107790194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31500178-G-T

107790404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31500037-C-T

107790649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499826-G-A

107790682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499791-C-T

107790691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499779-C-T

107790695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499775-T-A

107790712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499755-G-A

107790791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499660-T-C

107790847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499598-T-C

107790913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499415-T-C

http://identifiers.org/hco/7/GRCh38#107790918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31499410-A-C

107790918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499410-A-G

107790918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499410-A-T

107791105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31499193-G-A

107791105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31499193-G-T

http://identifiers.org/hco/7/GRCh38#107791108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31499190-A-C

107791115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31499183-A-G

107791260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499050-G-A

107791260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31499050-G-C

http://identifiers.org/hco/7/GRCh38#107791695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31498967-C-A

107791695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31498967-C-G

107791847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31498821-G-T

107791959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31498712-C-T

107791967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31498704-T-C

107793695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497956-G-T

107793850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31497758-G-A

107793939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497669-C-G

107793939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497669-C-T

http://identifiers.org/hco/7/GRCh38#107794229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31497372-C-A

107794237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497364-G-A

107794237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497364-G-T

http://identifiers.org/hco/7/GRCh38#107794284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31497316-C-A

107794287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497313-G-A

107794287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497313-G-C

107794287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497313-G-T

107794298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497302-G-T

107794308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31497292-A-G

107794396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31497209-A-G

107794396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31497209-A-T

107795233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31496254-G-A

107795603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31495597-G-A

107795735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31495489-C-T

107795827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31495401-T-C

107796489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31495113-C-T

107796578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31495032-T-C

107796839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31494807-A-T

107796993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31494586-C-G

107796993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31494586-C-T

107797000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31494579-A-T

http://identifiers.org/hco/7/GRCh38#107797888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31494097-A-C

107798293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31493692-C-T

http://identifiers.org/hco/7/GRCh38#107798485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31493497-A-C

107798682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31493360-C-G

107798857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31493191-C-G

107798929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31493122-G-A

107799964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31490770-T-C

107800410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31490472-A-G

107800612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31490330-A-G

107800821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31490120-G-A

107802321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31488957-C-T

107802497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31488794-G-T

107802696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31488748-T-C

107802790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31488657-A-G

107802790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31488657-A-T

http://identifiers.org/hco/7/GRCh38#107802982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31488463-A-C

http://identifiers.org/hco/7/GRCh38#107803150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#31488300-C-A

107803194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31488245-T-A

107803194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3018
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31488245-T-C