http://identifiers.org/hco/13/GRCh38#31846753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150042119-C-A

31846753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150042119-C-G

31846754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150042120-G-A

31846754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150042120-G-C

31846967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150042307-C-G

31847045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150042363-G-A

31847045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150042363-G-T

31847060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150042377-G-A

31847060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150042377-G-T

http://identifiers.org/hco/13/GRCh38#31847064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150042381-C-A

31847064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150042381-C-T

31847142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150042434-T-C

31847142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150042434-T-G

31847687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150042975-C-T

31847934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150043441-G-A

31848142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150043673-C-G

31848349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150043954-T-A

31848625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150044215-C-T

31848736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150044298-C-G

31849085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150044597-T-G

31849232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150044749-T-C

31849304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150044862-T-C

31849524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150045082-G-A

31849570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150045137-T-A

31849633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150045186-C-T

31849718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150045269-C-G

31849897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150045449-G-A

31849962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150045526-A-G

http://identifiers.org/hco/13/GRCh38#31849963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150045527-C-A

31849963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150045527-C-G

31850330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150046601-T-G

31850675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150047188-G-A

31850733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150047244-A-G

31850824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150047314-T-C

31851388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150048436-G-A

http://identifiers.org/hco/13/GRCh38#31851391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150048439-C-A

31851391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150048439-C-T

31851604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150048682-C-G

31851604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150048682-C-T

31851647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150048730-A-G

31851732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150048800-A-T

31851734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150048802-G-A

31851806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150048875-A-G

http://identifiers.org/hco/13/GRCh38#31852107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150049138-C-A

31852274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150049259-C-T

31852472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150049354-A-G

31852556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150049447-G-C

http://identifiers.org/hco/13/GRCh38#31852785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150049669-A-C

31852785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150049669-A-G

31856998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150051817-C-T

31857711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150052671-G-T

31857900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150052941-C-T

31857970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150053014-C-T

31858028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150053072-T-G

31858039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150053081-T-A

http://identifiers.org/hco/13/GRCh38#31858053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150053097-C-A

31858053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150053097-C-T

31858725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150053938-G-T

31858780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150053986-A-G

31859315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150054437-G-A

31859567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150054668-C-G

31859768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150054859-A-G

31860372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150055357-A-T

http://identifiers.org/hco/13/GRCh38#31860382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150055367-C-A

31860401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150055385-C-T

31860423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150055406-T-G

31860569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150055551-G-A

31860618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150055606-T-C

31860705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150055697-A-T

31861064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056006-G-A

31861177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056344-G-A

31861211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056381-G-A

31861211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056381-G-T

31861314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056491-G-A

http://identifiers.org/hco/13/GRCh38#31861378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150056552-A-C

31861378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056552-A-G

31861388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056559-A-G

31861411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056578-C-T

31861538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056688-T-G

31862641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056887-A-G

31862644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150056890-T-C

31862788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150057004-C-T

31862851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150057093-G-A

31862863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150057105-A-G

31862990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150057251-A-G

31863066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150057326-C-T

31863132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150057388-G-T

31863197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150057453-C-T

31863257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150057709-C-T

31865490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150058970-A-T

31865652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059109-A-T

http://identifiers.org/hco/13/GRCh38#31865660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150059117-C-A

31865871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059326-C-G

31865871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059326-C-T

31865900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059355-A-G

31865986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059448-G-A

31865986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059448-G-T

31866136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059586-A-G

31866270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059691-C-T

31866311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059728-C-T

31866357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059768-G-A

http://identifiers.org/hco/13/GRCh38#31866376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150059784-A-C

31866424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150059838-C-G

http://identifiers.org/hco/13/GRCh38#31867907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150061294-A-C

31867907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150061294-A-G

31870040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150062570-G-C

31870115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150062654-G-A

31870136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150062675-A-G

31870184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150062711-C-T

31870357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150062883-G-C

http://identifiers.org/hco/13/GRCh38#31870735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150063241-A-C

31871098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150063517-A-T

31871240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150063727-T-C

http://identifiers.org/hco/13/GRCh38#31871272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150063873-A-C

31871348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150063966-T-C

http://identifiers.org/hco/13/GRCh38#31871545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150064142-C-A

31871914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150064484-G-T

http://identifiers.org/hco/13/GRCh38#31872334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150064964-C-A

31872378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065009-T-G

31872411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065040-A-G

31872495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065147-A-G

31872581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065227-C-T

31872742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065372-G-T

31872886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065512-A-G

31872975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065715-T-C

31873072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065810-C-T

31873145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065878-T-C

31873208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150065939-C-T

31873408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150066109-T-G

31873649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150066313-T-C

http://identifiers.org/hco/13/GRCh38#31873679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150066343-C-A

31873878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150066488-G-A

31874189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150066763-A-G

31874217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150066785-G-A

http://identifiers.org/hco/13/GRCh38#31874261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150066863-A-C

31874261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150066863-A-G

31874320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150066921-G-A

31874320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150066921-G-T

31874597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150067598-A-G

31874617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150067620-A-G

31874816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150067833-G-A

31875028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150068011-A-G

31875140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150068122-C-T

31875183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150068165-T-C

31875290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150068272-C-T

31875565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150068558-G-A

31880599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150069819-A-G

31880637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150069857-G-A

31880673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150069898-C-G

31880691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150069916-C-G

http://identifiers.org/hco/13/GRCh38#31880718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150069943-C-A

31880718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150069943-C-G

31880737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150069962-T-C

31880790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070022-A-T

31880854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070100-G-A

31880992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070229-G-A

http://identifiers.org/hco/13/GRCh38#31881137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150070384-A-C

31881176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070426-G-A

31881433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070842-A-G

31881514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070873-A-T

31881559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070914-G-A

31881559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070914-G-C

31881579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070935-A-G

31881641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150070997-A-G

31881859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150071198-T-C

31882396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150073406-A-G

31882461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150073468-C-T

http://identifiers.org/hco/13/GRCh38#31882528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150073527-C-A

31882529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150073528-A-G

31882560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150073558-T-G

31882644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150073642-A-G

31884783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150074434-T-G

http://identifiers.org/hco/13/GRCh38#31884805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150074457-C-A

31884813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150074465-T-C

31885303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150074883-A-G

http://identifiers.org/hco/13/GRCh38#31885645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150075269-A-C

31885645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075269-A-G

31885899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075523-G-A

31886067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075662-C-T

31886141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075717-G-A

31886199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075775-A-G

31886246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075818-C-G

31886251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075823-C-T

31886345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075907-C-T

31886427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150075973-T-C

31886547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076085-C-T

31886718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076249-G-T

31886792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076295-G-A

31887008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076496-C-T

31887031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076519-A-G

31887031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076519-A-T

31887063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076535-T-A

31887063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076535-T-C

31887137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076595-T-C

31887262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150076728-G-T

http://identifiers.org/hco/13/GRCh38#31887331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150076786-A-C

31887527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077264-A-G

31887611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077350-T-C

31887634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077373-G-A

31887655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077394-A-G

31887759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077499-A-G

31887768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077508-A-G

31887774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077514-T-C

31887914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077630-G-A

31887934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077658-T-C

31887979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077702-C-T

31888051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077762-A-G

31888192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077870-C-T

31888214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150077892-C-T

31888501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078170-A-G

31888615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078245-A-G

31888800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078390-A-G

31888890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078465-C-T

31888898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078473-A-G

31888940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078515-T-C

31890745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078909-T-C

31890795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078948-A-G

31890803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078953-C-T

31890813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078963-T-C

31890824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150078974-G-C

31890920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079068-A-G

31891000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079152-C-T

31891026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079179-T-G

31891232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079401-C-T

31891354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079506-A-G

31891370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079522-G-A

31891370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079522-G-T

31891404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079538-G-A

31891404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150079538-G-T

31891478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080017-C-T

31891526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080059-G-T

31891609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080137-A-G

31891743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080268-C-T

31891751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080276-G-A

31891774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080299-G-A

31891833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080356-C-G

31891833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080356-C-T

31891992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080514-C-T

31891993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150080515-A-G

31892119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150081172-C-T

31892256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150081272-G-A

31892297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150081309-T-G

http://identifiers.org/hco/13/GRCh38#31892313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150081329-C-A

31893222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150081680-G-A

31893352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150081815-A-G

31893401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150081863-A-G

31893508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150081969-G-T

31896525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150082677-T-C

31896527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150082679-G-T

31896588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150082729-C-G

http://identifiers.org/hco/13/GRCh38#31896629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150082769-C-A

31896720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150082855-C-T

31897659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150083183-C-T

31897766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150083264-C-G

31898105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150083519-G-A

31898141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150083555-C-T

31898470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150083895-G-A

31898470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150083895-G-T

31898493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150083915-T-C

31898500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150083922-T-C

31898728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150084153-C-T

31898754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150084180-G-T

31899096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150084462-C-G

31899232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150084602-T-A

31899232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150084602-T-G

31899452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150084917-G-A

31899556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150085031-T-G

http://identifiers.org/hco/13/GRCh38#31899597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150085066-A-C

31899597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150085066-A-G

31901795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150085787-C-T

31902010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150086005-G-A

31902481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150086567-T-C

31902523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150086602-A-G

31902571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150086651-A-T

31904999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150086995-C-G

31905058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150087045-C-G

31905084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150087082-T-C

31905134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150087118-A-G

31905296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150087247-C-T

31905300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150087251-G-A

31905850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150088400-G-T

31905928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150088474-G-C

31905997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150088547-T-G

31906170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150088717-A-G

31906206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150088766-A-G

31906212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150088772-A-G

http://identifiers.org/hco/13/GRCh38#31906215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150088775-A-C

31906219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150088779-C-T

31906259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150088830-A-G

31908592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150090375-C-T

31908674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150090462-C-T

31908704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150090520-T-A

31908704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150090520-T-C

31908768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150090578-T-C

31908779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150090589-G-A

31909123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150090862-T-G

31909465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150091746-G-A

31909770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150092151-A-G

31909826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150092207-A-G

http://identifiers.org/hco/13/GRCh38#31910175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150092596-C-A

31910192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150092613-T-C

31912312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150092708-C-T

31912962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150093729-C-T

31914416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150094718-T-G

31914511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150094817-G-A

31915118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150095337-G-T

31915400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150095441-G-T

31915505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150095550-G-A

31915505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150095550-G-C

31915571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150095598-C-T

http://identifiers.org/hco/13/GRCh38#31915740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150095739-C-A

31917828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150096842-C-T

31917959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150096983-G-A

31917971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150096995-T-C

31918319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150097278-C-T

31918335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150097294-C-T

31918341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150097300-T-G

31918374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150097334-G-C

31918966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150098380-A-G

31919075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150098472-C-T

31919182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150098705-T-A

31926804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150099436-A-G

31927074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150099706-C-T

31927135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150099758-T-G

31927158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150099780-A-G

31927176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150099810-G-T

31927250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150099884-T-C

http://identifiers.org/hco/13/GRCh38#31927308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150099942-C-A

31927413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150100035-C-G

31927706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150100310-T-C

31928169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150101736-A-T

31928188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150101758-G-A

31928242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150101824-C-G

31929529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150103149-G-T

31929563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150103182-A-G

31929716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150103325-C-G

31929736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150103344-G-C

31929838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150103444-T-C

31929910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150103536-A-G

31929918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150103544-G-A

31930027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150103888-C-T

http://identifiers.org/hco/13/GRCh38#31930360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150104194-C-A

31930360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150104194-C-G

31930375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150104209-G-T

31930493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150104476-T-G

31930494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150104477-A-G

31930582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150104563-C-T

31930986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150104885-A-G

31931016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150104914-C-T

31931307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150105685-G-T

31931411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150105782-A-G

31931528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150105884-A-G

31931538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150105900-T-C

31931702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150106035-C-T

31931711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150106044-A-G

31931778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150106137-A-G

31931804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150106173-G-A

31931988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150106939-G-A

31932119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150107066-C-G

31933506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150108961-G-C

31933612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150109052-G-A

http://identifiers.org/hco/13/GRCh38#31934693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150109805-C-A

31935006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150110101-G-A

31935010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150110105-T-C

http://identifiers.org/hco/13/GRCh38#31935463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150110517-C-A

31935463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150110517-C-T

31935687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150110849-G-T

31939849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150111773-G-T

31940246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150112164-G-A

31940246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150112164-G-T

31940360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150112279-A-G

31940596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150112698-A-G

31940597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150112699-A-G

31940699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150112805-G-T

31940841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150112923-A-T

31940894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150112976-T-G

31941966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150115481-A-G

31942004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150115514-C-T

31942342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150115717-T-C

31942982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150116210-C-G

31943114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150116341-T-C

31943208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150116434-C-G

31943510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150117429-C-G

31943788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150117635-C-G

31943856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150117772-G-T

http://identifiers.org/hco/13/GRCh38#31943888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150117804-A-C

http://identifiers.org/hco/13/GRCh38#31943901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150117817-C-A

http://identifiers.org/hco/13/GRCh38#31944362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150118301-A-C

31944387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150118330-A-G

31945199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150119266-C-T

31945318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150119383-G-A

31945614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150119656-C-T

31945650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150119692-G-A

31945848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150119889-T-A

31945848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150119889-T-C

31945934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150119953-G-A

31946847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150120906-A-T

31947119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150121140-A-G

31947157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150121175-G-A

31948099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150123457-C-T

31948157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150123510-A-G

31948283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150123616-T-C

31948581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150123918-A-G

31948590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150123927-C-T

http://identifiers.org/hco/13/GRCh38#31948697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150124044-C-A

31948832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124164-A-G

31949273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124551-C-G

31949275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124553-C-G

31949362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124625-G-A

31949398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124668-T-A

31949398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124668-T-C

31949424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124707-C-T

31949649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150125152-G-T

31950408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125417-A-G

31950415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125424-G-A

31950417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125426-G-A

31950418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125427-G-A

31950420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125429-T-C

31950426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125435-A-G

31950483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125489-A-G

31950502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125508-A-G

31950521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125527-T-C

31950725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125793-A-G

31950799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125865-G-T

http://identifiers.org/hco/13/GRCh38#31950849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150125914-A-C

31950868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150125933-A-G

31950935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150126003-T-G

31950951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150126022-A-G

31950951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150126022-A-T

http://identifiers.org/hco/13/GRCh38#31951084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#150126581-C-A

31951084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126581-C-T

31951087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126584-G-A

31951158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126648-T-C

31951296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126770-A-G

31951315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126789-A-G

31951364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126845-A-G

31951388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126868-G-T

31951395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126875-T-C

31951396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126876-G-A

31951396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126876-G-T

31951398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126878-T-A

http://identifiers.org/hco/13/GRCh38#31951406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#150126886-C-A

31951406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126886-C-T

31951423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126903-T-A

31951423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150126903-T-C

31953486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127577-T-C

31953496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127585-T-C

31953518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127607-A-G

31953601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127695-G-T

31953617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127711-A-G

31955039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150128232-C-T

31955162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150128516-G-A

31955313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150128664-C-T

31955322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150128673-G-A

31955322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150128673-G-T

31957160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130535-A-G

31957193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130562-T-C

31957432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130763-C-T

31958738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150131406-T-A

31958742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150131410-T-A

31958791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150131457-C-T

31958960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150131645-G-A

31959437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150133711-A-G

31959512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150133781-T-C

31961780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150134417-G-A

31961780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150134417-G-C

31961780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150134417-G-T

31961814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150134456-T-C

http://identifiers.org/hco/13/GRCh38#31961885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150134510-C-A

31961885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150134510-C-T

31961912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150134536-G-A

31961927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150134551-T-C

http://identifiers.org/hco/13/GRCh38#31961979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150134607-C-A

31962030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150134653-T-C

31962055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150134678-G-T

http://identifiers.org/hco/13/GRCh38#31962086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150134708-C-A

31962210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150134844-A-G

31962953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150135934-G-T

31963321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150136258-C-T

31963636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150137124-T-A

31963977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150137465-C-T

31964235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150137704-G-A

31964590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150138092-A-G

31964668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150138348-T-G

31964711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150138405-C-G

31965739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150139557-G-A

31965961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150139792-G-A

31968499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150143815-T-A

31968506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150143830-C-G

31968514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150143838-A-G

31970055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150144560-G-A

31970796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145223-A-G

31970819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145246-A-G

31970863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145290-A-G

31970869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145296-A-G

31970869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145296-A-T

31970940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145368-A-G

31970940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145368-A-T

31971073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145495-A-T

31971128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145547-G-A

31971207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145626-C-T

31971298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145791-C-T

31971405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150145962-A-T

31971630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150146104-G-T

31972093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150146799-T-C

31972150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150146869-C-G

31972201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150146921-G-A

31972687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150147239-A-G

31973313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150147779-A-G

31973371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150149472-C-T

31973428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150149547-T-A

31977269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150150620-A-T

31977678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150150712-C-T

31977736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150150779-A-T

31977744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150150787-A-G

31978046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150151153-C-T

31978428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150151951-T-C

31978565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150152094-T-A

31978566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150152095-G-A

31978634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150152153-T-C

31978670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150152188-T-G

31993943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150152457-G-T

31994207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150152741-T-G

31997838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155179-C-T

31997855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155193-G-A

31997858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155196-A-G

31997929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155267-C-G

31997966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155302-C-T

31998002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155339-A-T

31998052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155380-T-G

31998070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155398-A-T

31998295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150155605-G-A

31998392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155697-G-T

31998420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155725-G-A

31998783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150155957-G-A

31998916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156065-G-A

31998925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156074-G-C

31998943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156092-C-G

31998998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156145-C-T

31999057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156204-G-T

31999122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156301-G-A

31999125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156333-G-A

32001215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150156611-A-G

32001278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156662-A-G

32001330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156708-A-G

32001414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150156772-G-A

32002926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150157254-G-C

32002978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150157299-A-G

32005270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150159750-A-G

32005285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150159775-A-T

32006913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150160706-G-A

32007005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150160789-A-G

32007215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150160968-G-A

32007221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150160974-A-G

32007418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150161182-A-G

32007643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150161635-G-T

32007681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150161672-C-T

32009622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150163568-C-T

32009624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150163570-C-T

32009755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150163696-G-C

32010473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150165324-A-G

32010508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150165360-G-T

32010569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150165419-C-G

32010569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150165419-C-T

32010605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150165455-C-G

32012573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150168594-A-G

32012645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150168666-A-G

32012746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150168764-C-G

32012818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150168835-G-A

32012899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150168912-G-A

http://identifiers.org/hco/13/GRCh38#32012997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150169011-A-C

http://identifiers.org/hco/13/GRCh38#32013003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150169017-A-C

32013181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150169132-C-T

32013422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150169366-T-C

32013613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150169435-A-G

32013632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150169446-C-T

32014197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150169894-G-A

32014235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150169929-C-T

32014254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150169933-G-A

32014362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150170026-A-T

32015052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150170436-C-T

http://identifiers.org/hco/13/GRCh38#32015143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150170497-C-A

32015307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150170628-G-A

32015324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150170638-T-C

32015409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150170708-C-T

32015588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150170887-T-C

32019290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150171134-A-G

32019803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150172204-A-T

32019850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150172248-T-C

http://identifiers.org/hco/13/GRCh38#32019858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150172256-C-A

32020014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150172400-A-G

32021693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150174327-C-T

32021829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150174453-A-G

32021857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150174478-G-T

32022116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150174887-G-A

32022186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150174960-C-T

32022206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150174979-C-T

32022236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150175009-A-G

32022417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150175182-G-C

32022537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150175292-G-A

32022667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150175414-T-C

32022931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150175686-A-T

http://identifiers.org/hco/13/GRCh38#32025690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150177412-C-A

http://identifiers.org/hco/13/GRCh38#32025766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#150177472-C-A

32025774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 150177481-T-C

http://identifiers.org/hco/13/GRCh38#32025962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#150177619-A-C

http://identifiers.org/hco/13/GRCh38#32026032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#150177682-C-A

32026060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 150177710-G-T

32026127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150177771-G-A

32026127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150177771-G-C

32026127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150177771-G-T

32026281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150177931-G-C

32026293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150177943-A-G

32026293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150177943-A-T

32026360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150178008-T-G

32026376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150178019-T-G

32027138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150179471-T-A

http://identifiers.org/hco/13/GRCh38#32027177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150179511-C-A

32027177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150179511-C-T

32027198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150179531-C-T

http://identifiers.org/hco/13/GRCh38#32027356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150179728-C-A

32027356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150179728-C-T

32027447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150179814-C-T

http://identifiers.org/hco/13/GRCh38#32027492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150179860-A-C

32027663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150180011-C-T

32027664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 150180012-T-A

32027664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 150180012-T-C

32027665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 150180013-G-A

32027674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 150180022-A-G

http://identifiers.org/hco/13/GRCh38#32027753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150180103-C-A

32028418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150180433-A-G

32028500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150180511-G-A

32028850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150181073-C-T

32029021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150181200-G-A

32029079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150181253-G-A

32029939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150181947-C-T

32030036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182019-C-T

32030113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182089-A-G

32030139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182122-T-G

32030405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182327-A-G

32030511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182456-T-C

32030571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182514-G-T

32030777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182701-A-G

32030829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182753-T-G

32030933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182848-T-G

32030980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150182882-A-G

32031049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150182946-A-G

32031063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150182957-T-G

32031157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183121-A-G

32031157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183121-A-T

http://identifiers.org/hco/13/GRCh38#32031330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#150183303-C-A

32031330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183303-C-T

http://identifiers.org/hco/13/GRCh38#32031394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150183343-C-A

32031394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150183343-C-T

32031403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150183352-A-G

32031521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150183476-A-G

http://identifiers.org/hco/13/GRCh38#32031588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150183546-C-A

32031658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150183612-G-A

32031876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150183814-G-A

32031876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150183814-G-T

32031917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150183867-A-G

32032100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150183992-C-T

32032163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150184054-C-T

32032351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150184264-T-A

32032784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150184692-G-C

http://identifiers.org/hco/13/GRCh38#32032816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150184726-A-C

32032900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150184807-G-A

32033127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150185022-G-A

32033370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150185275-T-C

32033421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150185321-A-G

32033457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150185365-G-A

32033530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150185418-C-T

32033804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150185710-G-A

32034024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150185940-T-G

32034218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186123-C-T

32034413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186332-C-T

32034486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186419-A-G

32034771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186659-G-A

32034771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186659-G-T

32034862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186743-G-A

32034977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186853-A-G

32035610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150187437-C-T

32035633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150187457-G-C

32035653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150187481-C-T

http://identifiers.org/hco/13/GRCh38#32035654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150187482-A-C

http://identifiers.org/hco/13/GRCh38#32036367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150188365-C-A

32036367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150188365-C-G

32036437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150188434-A-T

32036633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189133-G-A

32036633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189133-G-T

32036890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189561-C-G

32036974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189677-C-T

32037023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189765-G-C

32037048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189790-A-T

32037145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189902-A-G

32037176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150190070-C-G

32037939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190805-G-A

http://identifiers.org/hco/13/GRCh38#32037942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150190808-C-A

32037954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190818-C-G

32038113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190886-G-A

32038181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190909-C-T

http://identifiers.org/hco/13/GRCh38#32038221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150190949-A-C

32038664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150192037-T-C

32038875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150192579-A-G

32039016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150192668-A-G

32039034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150192686-T-C

32039252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150192954-C-T

32039309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150193006-A-G

http://identifiers.org/hco/13/GRCh38#32039375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150193434-A-C

32039396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150193460-G-A

32039441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150193502-A-G

32039586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150193604-T-G

32040319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150194338-G-A

32040451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150194558-T-C

32040666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150194854-G-A

32040764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150194951-C-T

32040832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150195018-C-G

http://identifiers.org/hco/13/GRCh38#32040833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150195019-A-C

32040921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150195094-C-T

32040957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150195115-C-T

32041162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150195307-T-C

32041275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150195424-A-T

32045903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150196469-G-T

32045973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150196533-C-T

32046026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150196586-T-G

http://identifiers.org/hco/13/GRCh38#32046138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150196697-C-A

http://identifiers.org/hco/13/GRCh38#32046166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150196725-C-A

32046166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150196725-C-T

32046168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150196727-T-A

32046521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150197031-G-T

32046683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150197180-T-C

32046770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150197302-T-C

32046781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150197313-G-C

32046891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150197490-A-G

32046911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150197509-G-C

32047773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150198827-A-G

32048113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150199196-C-T

http://identifiers.org/hco/13/GRCh38#32048830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150199884-A-C

32048830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150199884-A-G

32048983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150199977-C-T

32048991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150199985-C-T

32049126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150200130-A-G

32049287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150200245-T-G

32049398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150200319-T-A

32049619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150200377-G-A

32049750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150200504-T-C

32049789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150200546-T-C

32049880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150201206-T-C

32050099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150201746-A-G

32050154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150201803-A-T

32050317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150201955-G-A

32050872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202500-A-G

32050884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202520-C-T

32050950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202582-C-T

http://identifiers.org/hco/13/GRCh38#32051074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150202716-C-A

32051115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202761-C-T

32051116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202762-A-G

32051132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202778-G-A

32051222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202864-G-C

32051322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202961-T-C

32051332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150202971-A-G

32051435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150203069-A-G

32051562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150203161-G-T

32051672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150203249-G-C

http://identifiers.org/hco/13/GRCh38#32053233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150204481-C-A

32054095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150209021-C-T

http://identifiers.org/hco/13/GRCh38#32054099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150209025-C-A

32054291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150209182-T-C

32055859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150211399-G-A

32056403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150211618-C-T

32056404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150211619-A-T

32056430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150211645-A-G

32056595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150211785-G-T

32056703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150211885-T-C

32056761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150211943-A-G

32057093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150214795-G-C

32058245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150215491-A-G

32059789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150217775-C-T

32059852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150217837-A-G

32059868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150217851-T-G

32059885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150217868-A-G

32059885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150217868-A-T

32060461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150218523-A-G

32060672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150218737-G-C

http://identifiers.org/hco/13/GRCh38#32060936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150218961-C-A

32060936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 150218961-C-T

http://identifiers.org/hco/13/GRCh38#32061010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150219000-C-A

32061028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 150219018-C-G

32061200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219181-T-C

32061224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219202-T-A

32061224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219202-T-C

32061249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219242-G-T

32061310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219303-T-C

32061411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219403-G-T

32061458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219451-G-A

32061458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219451-G-T

32061459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219452-T-C

32061525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219519-G-A

http://identifiers.org/hco/13/GRCh38#32061687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150219668-A-C

32061687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219668-A-G

32061695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150219676-C-T

32061997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150220444-T-C

32062093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150220537-G-A

32062109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150220553-A-G

32062281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150220748-T-C

32062569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150221414-G-A

32062677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150221579-C-T

32062868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150221865-A-G

32062877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150221871-A-G

32062978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150221932-A-G

http://identifiers.org/hco/13/GRCh38#32063231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150222103-A-C

32063232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150222104-G-A

32063331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150222165-A-G

32063451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150222267-C-T

32063646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150222414-G-A

32063881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150222648-A-T

32063895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150222665-T-C

32063973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150222740-T-C

32064263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150222989-C-G

32064335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223035-G-C

32064339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223039-T-C

32064339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223039-T-G

32064383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223079-C-T

32064410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223119-C-T

32065027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223704-T-C

32065379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223895-C-G

32065412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223932-T-C

32065430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150223950-T-C

32065497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150224011-G-A

32065549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150224054-T-C

32065623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150224073-G-C

32065943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150224405-A-T

32066708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150225115-G-A

32066814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150225220-T-G

32067151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150225720-G-A

32067164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150225732-T-C

http://identifiers.org/hco/13/GRCh38#32067231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150225783-C-A

32067231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150225783-C-T

http://identifiers.org/hco/13/GRCh38#32067252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150225802-A-C

32067294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150225842-G-A

32067475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150225991-G-A

32068266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150226543-G-C

32068304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150226545-A-G

32068611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150226852-A-G

32068721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150226954-T-C

32072647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150228646-C-T

32073543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150229377-G-A

32073543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150229377-G-C

32073557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150229391-G-A

32076004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150230815-G-C

32076010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150230821-G-A

32076277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150231059-A-T

32078509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150233458-G-A

http://identifiers.org/hco/13/GRCh38#32078777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150233680-A-C

32078777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150233680-A-G

32078777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150233680-A-T

http://identifiers.org/hco/13/GRCh38#32078819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150233720-C-A

32078922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150233823-C-T

32078982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150233883-C-T

32082369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150235646-G-A

32082989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150236144-A-G

http://identifiers.org/hco/13/GRCh38#32083138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150236459-C-A

32083146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150236467-C-T

32083255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150236587-A-G

32083384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150236715-G-A

32083401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150236732-A-G

32083434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150236778-G-A

http://identifiers.org/hco/13/GRCh38#32083444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150236788-C-A

32083549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150236822-C-T

32084310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150237290-C-T

32084394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150237372-T-A

32084403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150237379-G-T

32084548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150237536-A-G

32086031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150238328-G-A

http://identifiers.org/hco/13/GRCh38#32086157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150238452-C-A

32086157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150238452-C-T

http://identifiers.org/hco/13/GRCh38#32086160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150238455-C-A

32086311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150238588-C-T

http://identifiers.org/hco/13/GRCh38#32086897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150238952-C-A

32086922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150238962-G-A

32087031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150239075-A-T

32087170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150239241-C-T

32087263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150239326-C-G

32087271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150239334-T-C

32087271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150239334-T-G

32087324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150239384-C-T

32087325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150239385-G-A

32088002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150239607-T-C

32088085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150239690-C-T

32088475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150240301-C-T

32088554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150240413-C-T

32088559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150240419-G-A

32088617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150240501-G-C

32089173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150242600-T-C

32089193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150242620-G-T

32089310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150242720-G-T

32089380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150242778-G-T

http://identifiers.org/hco/13/GRCh38#32089588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150242884-C-A

32089588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150242884-C-T

32089705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150242908-G-A

32089926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243017-G-A

32090030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243122-G-T

32090275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243308-A-G

32090284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243317-G-A

32090284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243317-G-C

http://identifiers.org/hco/13/GRCh38#32090296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150243334-C-A

32090346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243388-A-G

32090347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243389-T-A

32090347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243389-T-C

32090347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243389-T-G

32090399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243467-T-G

32090666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243714-A-G

32090679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150243727-G-A

http://identifiers.org/hco/13/GRCh38#32090687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150243735-C-A

32090990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150244068-G-C

32090993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150244071-C-T

32091236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150244308-A-T

32091508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150244517-T-C

32091584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150244594-C-G

32096204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150247427-G-A

32096223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150247447-T-A

32096223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150247447-T-C

32096306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150247531-G-C

32096350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150247573-G-A

32098292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150248772-T-G

32098584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249051-G-A

32098584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249051-G-C

http://identifiers.org/hco/13/GRCh38#32101827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150249464-C-A

32101851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249488-G-T

32101871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249511-G-A

32101871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249511-G-T

32101944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249577-A-G

32101944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249577-A-T

32101946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249579-A-G

32101946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249579-A-T

http://identifiers.org/hco/13/GRCh38#32101955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150249588-C-A

32101955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150249588-C-G

32101955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150249588-C-T

32101989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150249622-A-G

32102010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150249643-T-C

32102026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249666-A-G

32102031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150249671-T-C

http://identifiers.org/hco/13/GRCh38#32102068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150249706-C-A

http://identifiers.org/hco/13/GRCh38#32102153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150250083-C-A

32102153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150250083-C-T

http://identifiers.org/hco/13/GRCh38#32102156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150250086-C-A

32102156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150250086-C-T

32102159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150250089-T-G

32102173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150250103-G-A

http://identifiers.org/hco/13/GRCh38#32102210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150250140-C-A

32102297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150250234-C-T

32102344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150250861-A-T

32102377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150250894-A-G

32102796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150251470-G-A

http://identifiers.org/hco/13/GRCh38#32104003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150251975-C-A

32104164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150252129-G-A

32111016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150254702-A-G

32111153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256507-C-T

32111550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256573-G-A

32111652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256670-A-G

32111754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256747-G-A

32111757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256750-C-T

32111839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256825-T-C

32111847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256833-T-C

32111928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256913-T-C

32111931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150256916-C-G

32112419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150260064-G-A

32112571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150260202-T-C

32112633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150260263-T-C

32112752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150260369-C-T

32112794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150260437-T-C

32113085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150260860-G-A

32113121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150260907-A-T

32113429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150261214-A-G

32113780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150261554-G-A

32113883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150261663-G-A

32115056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263035-A-T

32115067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263046-T-C

32115088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263071-A-G

32116994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263486-G-A

http://identifiers.org/hco/13/GRCh38#32117049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150263537-A-C

32117049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263537-A-G

32117117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263605-C-G

32117219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263691-T-C

32117236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263708-T-C

32117254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263726-G-C

32117254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263726-G-T

32117293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150263773-A-T

32117456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150263940-A-T

http://identifiers.org/hco/13/GRCh38#32117529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150264129-A-C

32117838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264443-A-G

32117838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264443-A-T

32117877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264481-G-A

32117934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264507-G-C

32117934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264507-G-T

32117945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264514-C-T

32117980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264546-C-T

http://identifiers.org/hco/13/GRCh38#32117981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150264547-A-C

32117981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264547-A-G

http://identifiers.org/hco/13/GRCh38#32118052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150264603-C-A

http://identifiers.org/hco/13/GRCh38#32118084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150264635-C-A

32118091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150264642-A-G

32118501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150265290-C-G

32118764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150265931-T-A

32118764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150265931-T-C

http://identifiers.org/hco/13/GRCh38#32118854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150266014-A-C

32118854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150266014-A-G

32118931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150266095-T-C

32119019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150266199-C-T

32119277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150266662-G-T

32119318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150266706-G-A

32119340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150266717-A-G

32119752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150267454-T-A

32119755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150267457-C-T

32120190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150267936-A-G

32124352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150269084-A-G

32124392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269124-A-G

http://identifiers.org/hco/13/GRCh38#32124424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150269150-A-C

32124545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269257-G-A

32124545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269257-G-C

http://identifiers.org/hco/13/GRCh38#32124568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150269281-C-A

32124568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269281-C-G

32124568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269281-C-T

http://identifiers.org/hco/13/GRCh38#32124569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150269282-C-A

32124588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269301-C-T

32124622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: 150269336-A-G

32124637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150269351-T-C

http://identifiers.org/hco/13/GRCh38#32124730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150269448-A-C

32124730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269448-A-T

32124746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269464-T-G

32124755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269473-G-T

32124889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269605-A-G

32124924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269624-T-C

32124925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269625-G-A

32124925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150269625-G-C

32126128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150271909-G-T

32126240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150272037-C-T

32129608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150275432-G-A

http://identifiers.org/hco/13/GRCh38#32129641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150275455-C-A

32129665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150275478-T-C

http://identifiers.org/hco/13/GRCh38#32129688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150275500-A-C

32129709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150275520-T-G

32129878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150275618-G-A

32129905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150275645-T-A

32131222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277513-G-A

32131329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277619-G-A

32131417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277714-T-G

32131462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277753-G-T

http://identifiers.org/hco/13/GRCh38#32131524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150277810-A-C

32131543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277829-A-G

http://identifiers.org/hco/13/GRCh38#32131547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150277833-C-A

32131547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277833-C-T

32131579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277849-T-C

http://identifiers.org/hco/13/GRCh38#32131589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150277859-C-A

32131589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277859-C-T

32131609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150277879-A-G

32132213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150279178-C-G

http://identifiers.org/hco/13/GRCh38#32132232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150279197-A-C

32132239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150279204-A-G

32132432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150279314-C-T

32132513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150279394-C-T

32132944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150280705-A-G

32133002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150280759-G-C

32133477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150281356-T-C

32133595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150281475-G-A

32133595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150281475-G-T

32134465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150281882-A-T

32134702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282080-C-G

32134802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282178-A-T

32134856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282216-T-C

http://identifiers.org/hco/13/GRCh38#32134866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150282226-C-A

32134866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282226-C-G

http://identifiers.org/hco/13/GRCh38#32134869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150282229-A-C

32134869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282229-A-G

32134869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282229-A-T

32134942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150282302-T-C

32134987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150282347-A-G

http://identifiers.org/hco/13/GRCh38#32135241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150282610-A-C

32135241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282610-A-G

32135268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282637-G-A

http://identifiers.org/hco/13/GRCh38#32135292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150282660-C-A

32135335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282685-G-A

32135335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282685-G-T

32135540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282889-G-T

32135585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150282935-G-A

32135779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150283081-G-A

32135883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150283181-G-T

32135992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150283280-A-T

32136036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150283323-A-T

32136131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150283430-A-G

http://identifiers.org/hco/13/GRCh38#32136202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150283481-A-C

32136222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150283501-G-A

32136261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150283542-G-A

32136525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284251-C-T

32136663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284397-G-T

32136767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284477-C-G

32136767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284477-C-T

32136771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284481-G-A

32136771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284481-G-T

32136847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284556-T-C

32136867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150284576-T-A

32136867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150284576-T-C

32136867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150284576-T-G

32137135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284803-T-C

32137192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150284878-A-T

32137569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150285419-G-A

32137635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150285499-T-G

32137693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150285529-T-C

32137841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150285662-C-T

32137901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150285741-T-C

32138027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150285866-A-T

32138111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150285948-C-T

32138458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150287931-T-G

32138659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150288147-T-A

32138992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150288773-G-T

32139063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150288846-T-C

32139094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150288877-G-T

32139177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150288961-T-C

http://identifiers.org/hco/13/GRCh38#32139344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150289105-C-A

32139509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150289247-A-G

32139550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150289284-A-G

32139580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150289314-C-G

32139745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150289479-T-C

32140040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150289736-A-G

32143123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150290262-G-C

32143690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150290919-C-T

http://identifiers.org/hco/13/GRCh38#32146791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150292488-C-A

32146802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150292499-G-C

32147009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150292679-C-T

32147114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150292781-C-T

32147174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150292840-C-T

32147183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150292849-T-G

32147184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150292850-G-A

32147202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150292866-G-A

32147202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150292866-G-T

32147305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150292957-A-G

32147406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293058-A-G

32147415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293067-A-T

32147458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293174-T-A

32147461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293177-G-T

http://identifiers.org/hco/13/GRCh38#32147462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150293178-C-A

32147462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293178-C-T

32147506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293221-T-A

32147506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293221-T-C

32147606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293281-G-C

32147606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293281-G-T

32147607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293282-A-G

32147720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293431-G-T

32147741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293468-T-C

http://identifiers.org/hco/13/GRCh38#32147761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150293513-A-C

http://identifiers.org/hco/13/GRCh38#32147914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150293667-C-A

http://identifiers.org/hco/13/GRCh38#32147995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150293722-C-A

32147995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293722-C-T

http://identifiers.org/hco/13/GRCh38#32147998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150293725-C-A

32147998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293725-C-G

32147998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293725-C-T

32148035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293755-T-C

32148053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293773-G-A

32148053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293773-G-T

32148055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293775-G-T

32148117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150293833-C-T

32148440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150294232-G-A

32148517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150294363-G-A

32149002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150295059-C-G

32149669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150295894-T-C

32149669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150295894-T-G

http://identifiers.org/hco/13/GRCh38#32149721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150295945-C-A

http://identifiers.org/hco/13/GRCh38#32149742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150295981-C-A

32149873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296106-T-A

32149893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296128-G-A

32149893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296128-G-T

http://identifiers.org/hco/13/GRCh38#32149902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150296161-C-A

32149902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296161-C-T

32149926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296204-T-C

32149952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296229-T-C

32149959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296236-A-G

32150049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296313-C-G

32150070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296334-A-T

32150369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296503-G-A

32150502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296647-C-T

32150855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150296997-A-G

32151157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150297206-C-T

32151239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150297843-C-G

32151268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150297872-C-T

32151536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150299064-G-A

32151578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150299106-G-A

32151701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150299223-G-A

32151785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150299309-G-A

32151874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150299483-A-G

32151952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150299681-C-T

32152087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150299814-A-G

32152150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150299868-G-A

32152244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300164-C-T

32152272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300196-C-G

32152322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300246-G-A

32152437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300325-T-A

32152460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300340-A-T

http://identifiers.org/hco/13/GRCh38#32152573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150300442-C-A

32152636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300506-G-A

32152718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300594-A-T

32152743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300619-A-T

32152949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300812-T-A

32152949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300812-T-C

32153043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150300906-C-T

32154959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150301166-A-T

32155553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150302336-G-A

32155553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150302336-G-C

32155559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150302342-T-C

32155583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150302366-T-C

32155698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150302454-T-A

32155701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150302457-G-A

32155701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150302457-G-T

http://identifiers.org/hco/13/GRCh38#32155702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150302458-C-A

http://identifiers.org/hco/13/GRCh38#32155756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150302510-C-A

32155792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150302569-A-T

32156134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150302870-T-A

32156222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150302956-T-C

32156240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150302974-T-C

32157159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150304139-A-G

32157172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150304158-A-T

32157209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150304198-G-T

32157219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150304208-G-A

32157219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150304208-G-T

32157232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150304224-T-A

32157325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150304315-G-A

32157325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: 150304315-G-T

32160964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150304905-A-T

32160981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150304922-G-T

http://identifiers.org/hco/13/GRCh38#32161024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150304963-C-A

http://identifiers.org/hco/13/GRCh38#32161083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150305011-C-A

http://identifiers.org/hco/13/GRCh38#32161102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150305041-C-A

32161189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150305126-T-A

32161255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150305192-G-A

32162681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150307343-A-G

32163048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150307808-T-C

32163048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150307808-T-G

32163056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150307816-T-C

32163483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150308183-A-G

32163517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150308226-T-A

http://identifiers.org/hco/13/GRCh38#32163754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150308454-C-A

32163754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150308454-C-T

32164043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150308693-G-C

32164226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150308870-T-C

32164457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150309090-C-T

32164698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150309301-G-A

32170972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150309415-A-G

32171012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 150309450-G-A

32171012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 150309450-G-C

32171012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 150309450-G-T

32171102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: 150309540-T-G

http://identifiers.org/hco/13/GRCh38#32171623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150310133-C-A

http://identifiers.org/hco/13/GRCh38#32171680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150310191-A-C

http://identifiers.org/hco/13/GRCh38#32172407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150310373-A-C

32172731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150310647-T-C

32172749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150310656-C-T

32172857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150310754-T-C

32173120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150312011-G-A

http://identifiers.org/hco/13/GRCh38#32173230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150312123-C-A

32173230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150312123-C-T

32173361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150312232-T-C

32173362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150312233-A-G

32173543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: 150312414-G-C

http://identifiers.org/hco/13/GRCh38#32175398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#150313962-C-A

32175494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150314049-G-A

32175494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, undefined
orthologous variants: 150314049-G-C

32175671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150314233-G-A

32175671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150314233-G-T

32175729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150314292-T-A

http://identifiers.org/hco/13/GRCh38#32175749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150314312-C-A

32175762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150314325-T-C

32175762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150314325-T-G

32175965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150314514-G-A

32175965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150314514-G-C

http://identifiers.org/hco/13/GRCh38#32176253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150315096-C-A

32176268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315111-T-C

32176287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315130-G-A

32176287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315130-G-C

32176314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315157-G-A

32176336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315181-C-G

32176336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315181-C-T

32176339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315184-G-C

http://identifiers.org/hco/13/GRCh38#32176341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150315186-C-A

32176346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315191-C-T

32176378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315223-G-A

32176441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315278-C-G

32176589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315385-C-T

32176650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315447-G-A

32176735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150315525-C-T

http://identifiers.org/hco/13/GRCh38#32176862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150315611-A-C

http://identifiers.org/hco/13/GRCh38#32176880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150315627-A-C

32177282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150316207-T-C

32178063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317331-G-A

32178063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317331-G-T

http://identifiers.org/hco/13/GRCh38#32178065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150317333-C-A

32178077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317351-G-A

32178077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317351-G-T

32178095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317369-A-G

32178101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317375-T-C

32178102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317376-A-T

32178160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317428-A-G

32178329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150317595-C-T

32178498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317754-A-T

32178505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317761-G-A

32178505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317761-G-C

32178505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317761-G-T

32178527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317783-T-C

http://identifiers.org/hco/13/GRCh38#32178536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150317796-C-A

32178587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317846-T-A

32178587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317846-T-C

32178606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317870-T-G

32178662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317931-G-A

32178698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150317964-T-A

32178804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150318415-G-A

32178804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150318415-G-T

http://identifiers.org/hco/13/GRCh38#32178819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150318430-C-A

32178838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150318447-T-C

32178985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150318594-A-G

32179074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150318684-T-C

32179150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150318765-T-C

32179266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150318874-A-G

32179440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319006-A-T

http://identifiers.org/hco/13/GRCh38#32179445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150319011-A-C

32179445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319011-A-G

32179445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319011-A-T

32179500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319061-A-T

32179543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319106-T-G

32179561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319127-T-A

32179561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319127-T-C

32179710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150319243-G-A

32179816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319349-G-C

32179816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319349-G-T

32179829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319361-T-C

32179846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319378-T-G

32179881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319414-G-T

32179891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319427-G-A

32179891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319427-G-T

32179904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319449-G-T

32180120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150319620-T-G

32181816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150320148-G-A

32181816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150320148-G-C

32181825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150320153-T-C

32181913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150320233-G-T

32181917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150320237-A-T

32181941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150320262-A-G

32182223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150320476-G-A

32182395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321218-A-G

32182478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321292-C-T

32182492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321304-C-T

32182508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321320-G-A

32182508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321320-G-T

32182543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321349-G-A

32182660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321467-G-A

32182849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321543-G-A

32182849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321543-G-T

http://identifiers.org/hco/13/GRCh38#32182886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150321578-A-C

32182916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321602-T-C

32183135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321821-C-T

32183136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321822-A-T

http://identifiers.org/hco/13/GRCh38#32183137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150321823-C-A

32183137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321823-C-T

32183158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321846-A-G

32183304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321958-T-C

32183309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150321963-G-A

32184304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322410-G-A

32184327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322433-G-A

32184403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322506-T-C

32184417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322516-C-T

32184488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322583-G-A

32184488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322583-G-T

http://identifiers.org/hco/13/GRCh38#32184518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150322613-C-A

32184518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322613-C-T

32184566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322638-G-A

32184566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322638-G-T

http://identifiers.org/hco/13/GRCh38#32184595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150322659-C-A

32184595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150322659-C-T

32184638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150322702-A-G

32184638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150322702-A-T

32184686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: 150322750-T-A

32184686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150322750-T-C

32184686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: 150322750-T-G

http://identifiers.org/hco/13/GRCh38#32184689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150322753-C-A

32184689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 150322753-C-T

32184714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322775-T-A

32184758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322804-T-C

32184758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322804-T-G

32184823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322866-G-A

32184823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322866-G-C

32184823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322866-G-T

32184882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322921-G-C

32184911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322949-A-G

32184916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322954-G-A

http://identifiers.org/hco/13/GRCh38#32184917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150322955-C-A

32184954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322977-G-A

32184954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322977-G-C

32184954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150322977-G-T

32185009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150323030-C-T

32185063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150323084-T-C

32185063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150323084-T-G

32186244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150324242-G-T

http://identifiers.org/hco/13/GRCh38#32186345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150324343-C-A

32186348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150324346-T-C

32186357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150324355-T-C

32187605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150325124-T-C

32187732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150325223-G-A

32187734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150325225-A-G

32187736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150325227-T-C

32187736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150325227-T-G

32187744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150325235-A-G

32187806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150325296-T-A

32187806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150325296-T-C

32192641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150326561-A-G

32192641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150326561-A-T

http://identifiers.org/hco/13/GRCh38#32194103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150326869-C-A

32194103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150326869-C-T

32194131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150326895-C-G

32194131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150326895-C-T

32194211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150326975-T-C

32194238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150327002-A-G

http://identifiers.org/hco/13/GRCh38#32194250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150327014-A-C

32194250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150327014-A-G

32194256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150327020-A-G

32194309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327074-T-A

32194309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327074-T-C

32194338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327103-T-C

32194452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327211-C-G

32194512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327265-G-C

32194594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327347-G-A

32194736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327471-G-C

32194737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327472-A-T

32194773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327595-T-C

32194965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150327784-A-T

32201808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328284-G-T

32201881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328358-A-G

32201909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328381-G-C

32201909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328381-G-T

32201917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328385-T-C

32201917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328385-T-G

32201931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328398-G-A

32201931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328398-G-T

http://identifiers.org/hco/13/GRCh38#32201953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150328420-C-A

32201953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150328420-C-T

32202016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150328483-T-C

32202057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328522-G-A

32202057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328522-G-T

32202058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328523-G-A

32202080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328546-A-G

32202173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328573-T-A

32202173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328573-T-G

32202174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328574-G-A

32202174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328574-G-T

32202234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328619-T-G

http://identifiers.org/hco/13/GRCh38#32202245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150328630-A-C

32202263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328646-T-C

32202352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150328711-A-G

32202541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150328900-G-T

http://identifiers.org/hco/13/GRCh38#32203807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150329829-C-A

http://identifiers.org/hco/13/GRCh38#32204054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150330075-A-C

32205751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150332468-G-C

32205787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150332493-G-A

32205844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150332545-G-A

32206067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150332728-G-A

32206169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150332779-C-T

32206462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333010-T-C

http://identifiers.org/hco/13/GRCh38#32206724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150333257-C-A

32206724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333257-C-T

32206809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333333-T-C

32206871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333393-G-A

32206871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333393-G-T

32206900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333423-A-G

32207037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333545-G-C

32207246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333732-G-C

32207272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333762-G-A

http://identifiers.org/hco/13/GRCh38#32207305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150333795-C-A

32207305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333795-C-T

32207428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150333899-C-T

32208497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336339-C-G

32208563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336389-C-T

32208575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336401-C-T

http://identifiers.org/hco/13/GRCh38#32208784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150336582-C-A

32208784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336582-C-T

32208808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336610-T-G

32208824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336626-T-G

32208926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150336722-G-A

32209137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336916-T-G

32209142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336921-T-C

32209182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336969-C-T

32209197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150336984-T-A

32209374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150337785-A-T

32209428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150337838-C-G

32209471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150337879-T-C

http://identifiers.org/hco/13/GRCh38#32209498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150337904-C-A

32209553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150337932-C-T

32209582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150337966-T-C

32209620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150338004-T-C

32209644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150338028-T-C

32209644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: 150338028-T-G

32209647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150338031-G-A

32209647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: missense variant
orthologous variants: 150338031-G-C

32209674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150338058-C-G

32209674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150338058-C-T

32209722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150338106-C-T

32209759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150338131-G-A

http://identifiers.org/hco/13/GRCh38#32209878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150338183-C-A

32209878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150338183-C-T

32209973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150338274-T-C

32209987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150338283-G-C

32210261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150338708-T-G

32210327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150338761-G-A

32210351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150338784-C-T

32210598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339397-A-G

32210653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339462-G-A

32210717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339520-T-G

32210750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339551-A-G

32210759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339560-A-G

32210774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339571-T-C

32210775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339572-G-A

32210775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339572-G-T

32210836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339622-A-G

32211003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150339790-G-A

32211003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150339790-G-C

32211030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: synonymous variant
orthologous variants: 150339817-C-T

http://identifiers.org/hco/13/GRCh38#32211074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150339850-C-A

32211074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339850-C-T

32211132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339896-T-C

32211207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339967-C-T

32211229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150339988-G-A

http://identifiers.org/hco/13/GRCh38#32211458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150340457-C-A

32211493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150340515-A-T

http://identifiers.org/hco/13/GRCh38#32211530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150340551-A-C

32211694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150341223-A-T

32211791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150341309-C-T

32211967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150341492-A-G

32212159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150341802-G-A

32212179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150341821-C-T

http://identifiers.org/hco/13/GRCh38#32212242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#150341883-C-A

32212242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20367
most severe consequence: intron variant
orthologous variants: 150341883-C-T