130212832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105928892-G-A

130213053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105928695-A-G

130213056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105928692-A-G

http://identifiers.org/hco/3/GRCh38#130213175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105928582-C-A

130213395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105928360-G-T

130213730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105928261-C-T

http://identifiers.org/hco/3/GRCh38#130213736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105928255-C-A

130214246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105927025-G-A

130214246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105927025-G-T

130214332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105926941-G-T

130214569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105926730-T-A

130214695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105926618-T-G

130214741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105926571-C-T

130214850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105926467-G-C

130214861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105926456-C-T

130214939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105926373-A-G

130215620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105924999-C-T

130215693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105924932-G-C

130218124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105921615-A-G

http://identifiers.org/hco/3/GRCh38#130218136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105921603-C-A

http://identifiers.org/hco/3/GRCh38#130218239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105921506-C-A

130218461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105921304-G-A

130218461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105921304-G-T

130218495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105921275-C-G

130218757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105921034-T-C

130219194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105920114-C-T

http://identifiers.org/hco/3/GRCh38#130219549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105919749-C-A

130219549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919749-C-T

http://identifiers.org/hco/3/GRCh38#130219552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105919746-C-A

130219713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919599-G-A

130219762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919550-G-T

130219806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919506-G-A

130219875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919459-A-G

130219919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919429-G-A

130219919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919429-G-C

130219919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919429-G-T

130219928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919420-G-C

130220032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919305-G-A

130220048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105919283-C-T

130221197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105918507-T-C

130221230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105918489-A-G

130221249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105918479-T-G

130221299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105918435-T-C

130221443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105918285-A-G

130221480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105918247-G-T

130221704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105917975-T-C

130221772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105917851-A-G

130221906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105917725-G-T

130221928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105917659-G-T

130221958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105917631-G-T

130222092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105917464-G-T

http://identifiers.org/hco/3/GRCh38#130222490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105917084-A-C

130222787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105916817-C-T

130222948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105916669-A-T

130222950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105916667-C-G

130223097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105916530-G-T

http://identifiers.org/hco/3/GRCh38#130223223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105916414-C-A

130223229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105916408-C-T

130223668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105916257-A-T

130223684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105916239-A-G

130223764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105916162-A-G

130225905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105915107-A-G

130226081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105914876-T-A

130226081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105914876-T-G

130226124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105914833-A-G

130226552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105914483-A-G

130227611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

130227889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105911305-A-T

http://identifiers.org/hco/3/GRCh38#130227890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105911304-C-A

130231187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907512-A-G

130231258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907430-C-T

130231304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907379-A-G

http://identifiers.org/hco/3/GRCh38#130231322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105907361-C-A

130231322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907361-C-T

130231323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907360-A-G

130231377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907304-A-G

130231414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907269-G-T

130231540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907135-A-G

130231578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907099-T-C

130231642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907042-A-G

130231670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105907014-A-G

130231790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105906896-G-T

130232256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105906598-T-C

130232611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105906270-A-G

130232620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105906261-C-T

130232782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105906096-C-T

130233110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905775-A-G

130233179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905712-A-G

130233212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905679-A-G

130233214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905677-A-G

130233274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905614-G-A

130233371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905524-G-T

http://identifiers.org/hco/3/GRCh38#130233387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105905508-C-A

130233390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905505-G-T

130233414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905481-T-C

130233557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905334-A-G

130233562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905329-T-C

130233578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905313-T-C

130233826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905092-C-T

130233917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105905008-G-A

130234076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105904851-A-G

130234401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105904349-A-G

http://identifiers.org/hco/3/GRCh38#130234468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105904286-C-A

130234598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105903704-G-A

130234665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105903637-C-T

130234678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105903366-G-T

http://identifiers.org/hco/3/GRCh38#130234837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105903182-A-C

130234970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105902951-A-G

130235044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105902864-A-G

http://identifiers.org/hco/3/GRCh38#130235220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105902690-C-A

130235648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105902529-A-G

130235739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105902443-G-A

130235868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105901756-T-C

130235890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105901734-A-G

130235970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105901656-T-C

130236115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900838-G-A

130236154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900792-C-T

130236209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900758-T-C

130236209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900758-T-G

130236246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900721-T-C

130236306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900642-G-T

130236342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900612-T-C

http://identifiers.org/hco/3/GRCh38#130237377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105900266-A-C

130237483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900159-T-C

http://identifiers.org/hco/3/GRCh38#130237491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105900151-C-A

130237491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900151-C-T

130237512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105900128-T-C

130237588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105900054-G-A

130243647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105898445-A-G

130243780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105898318-T-A

130244046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105898080-C-T

130244128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105898057-G-A

130244347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897942-G-A

130244347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897942-G-T

130244389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897902-A-T

130244440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105897852-G-T

http://identifiers.org/hco/3/GRCh38#130244596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105897736-C-A

130244596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897736-C-T

http://identifiers.org/hco/3/GRCh38#130244605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105897727-C-A

130244605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897727-C-T

130244967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897499-T-C

130245085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897359-G-T

130245139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897299-A-G

130245338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105897098-A-T

130245568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105896838-G-T

130245578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105896823-G-T

130245599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105896804-A-G

130245606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105896800-G-T

130245764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105896672-T-C

130246003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105896446-A-T

130246312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105896180-C-T

http://identifiers.org/hco/3/GRCh38#130246401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105895700-C-A

130246589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105895523-A-G

130246678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105895436-G-A

130246963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105895158-T-C

130247004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105895117-T-C

130247472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105894957-T-C

130247544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105894890-T-C

130247555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105894880-T-C

130247961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105894134-C-T

130248065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105894033-C-G

http://identifiers.org/hco/3/GRCh38#130248287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105893821-C-A

130248423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 105893692-G-A

130248423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 105893692-G-C

130248427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105893688-G-A

130248483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105893647-A-G

http://identifiers.org/hco/3/GRCh38#130248500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105893630-C-A

http://identifiers.org/hco/3/GRCh38#130248684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105893445-C-A

130248684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105893445-C-T

http://identifiers.org/hco/3/GRCh38#130248705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105893421-C-A

130248705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105893421-C-T

130248990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105893171-T-C

http://identifiers.org/hco/3/GRCh38#130249137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105893030-A-C

130249211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105892967-T-A

130249215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105892963-T-C

130249313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105892866-A-G

130249438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105892745-G-T

130249705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105892240-C-T

130249706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105892239-A-G

130249710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105892235-A-G

130249845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105892090-G-A

130250638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105891255-G-A

130250638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105891255-G-T

130250823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105890989-T-C

130250884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105890928-C-T

130250926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105890886-T-C

http://identifiers.org/hco/3/GRCh38#130250943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105890869-A-C

http://identifiers.org/hco/3/GRCh38#130250971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105890841-C-A

130250971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105890841-C-T

130251108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105890704-G-A

130251108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105890704-G-T

http://identifiers.org/hco/3/GRCh38#130251230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105890580-C-A

130251230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105890580-C-T

130251241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105890569-G-T

130251319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105890487-G-A

130251350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105890436-G-A

130251394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105890372-A-G

130251448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105890318-G-A

130251448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105890318-G-T

130251519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105890248-C-T

http://identifiers.org/hco/3/GRCh38#130251566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105890209-A-C

130251566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105890209-A-G

http://identifiers.org/hco/3/GRCh38#130251592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105890183-A-C

http://identifiers.org/hco/3/GRCh38#130251679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105890100-C-A

130251776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105890009-T-C

130251930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105889644-T-A

130251941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105889515-C-G

130251960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105889496-C-T

130252137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105889327-T-C

130252616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105888842-G-T

130252619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105888839-G-T

130252705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105888756-T-G

130252764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105888694-G-C

130253066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105888128-G-C

130253155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105888041-A-G

130253640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105887571-T-C

130253667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105887544-T-G

130253670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105887541-A-G

130255641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105887238-G-C

130255641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105887238-G-T

130255731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105887153-A-G

130256955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105885882-A-G

130256997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105885843-T-A

130257055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105885782-G-A

130257259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105885569-C-T

130257686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105883266-G-A

130257709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105883249-G-A

130257931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105883010-T-C

130258139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882797-C-G

130258139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882797-C-T

130258450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882502-C-T

130258477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882474-C-T

130258570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882389-A-G

130258691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882273-G-T

130258717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882248-T-C

130258923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882050-C-G

130258923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105882050-C-T

130259024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105881960-T-A

130259028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105881956-T-C

130259064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105881942-C-T

130259401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105881642-C-T

130259425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105881618-A-G

130259804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105881255-C-T

130260026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105881069-A-T

130260131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105880981-C-T

130260229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105880912-T-A

130260774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105880571-A-G

130260784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105880559-A-G

130261336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105880029-G-T

130261368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105880007-G-A

130261595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105879796-T-C

130261694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105879737-C-T

130261859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105879603-T-C

130261887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105879578-A-G

130261954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105879518-A-G

130263443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105878632-A-T

130263653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105878260-T-C

130263686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105878227-G-T

130263690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105878223-G-T

130263693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105878220-A-G

130263732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105878184-T-C

130263831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105878061-T-C

130263838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105878054-C-G

130263838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105878054-C-T

130263848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105878044-A-G

130263850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105878042-G-T

http://identifiers.org/hco/3/GRCh38#130263985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105877907-C-A

130263985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105877907-C-G

130263985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105877907-C-T

130263994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105877898-C-T

130264094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105877798-A-G

130264112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105877780-T-A

130264245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105877648-G-A

http://identifiers.org/hco/3/GRCh38#130264314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105877579-C-A

130264384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105877509-T-C

130264755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105876829-A-G

130265038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105876564-A-T

130265177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105875859-T-C

130265309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105875760-C-T

130265417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105875652-G-A

130265469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105875608-G-A

130265724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105875367-A-G

130266288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105874400-C-T

130266299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105874389-C-T

130266781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105873596-C-G

130266781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105873596-C-T

130267114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105873229-A-G

130267135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105873208-G-A

http://identifiers.org/hco/3/GRCh38#130267474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105872859-C-A

130267474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105872859-C-T

130267544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105872813-G-A

130267544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105872813-G-C

130267544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105872813-G-T

130268008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105872472-A-G

130268152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105872110-A-G

http://identifiers.org/hco/3/GRCh38#130268496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105871713-A-C

130268549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105871661-A-G

130268600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105871079-T-A

http://identifiers.org/hco/3/GRCh38#130268652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105871031-A-C

http://identifiers.org/hco/3/GRCh38#130268671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105871010-C-A

130268671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105871010-C-T

130268724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105870960-A-G

130268866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105870831-G-A

130268916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105870792-T-C

http://identifiers.org/hco/3/GRCh38#130268978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105870734-C-A

130268994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105870719-C-T

http://identifiers.org/hco/3/GRCh38#130269020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105870693-C-A

130270995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105870137-A-G

http://identifiers.org/hco/3/GRCh38#130271006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105870133-A-C

130271068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105870072-C-T

130271272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869860-C-G

130271272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869860-C-T

130271319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869817-T-C

130271322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869814-A-G

130271347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869791-G-A

130271516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869625-T-C

http://identifiers.org/hco/3/GRCh38#130271570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105869568-A-C

130271718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869439-A-G

130271732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869425-G-A

130271905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869266-T-A

130272031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869171-A-G

130272032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869170-C-G

130272159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869063-A-T

130272176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869046-A-G

130272181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105869041-A-G

130272253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868988-C-T

130272286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868955-C-T

http://identifiers.org/hco/3/GRCh38#130272483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105868695-A-C

130272603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868593-T-C

130272911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868231-T-C

130272928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868214-C-T

130272929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868213-A-G

130272995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868151-G-A

http://identifiers.org/hco/3/GRCh38#130273009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105868137-C-A

130273021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868125-G-T

130273074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868073-A-G

http://identifiers.org/hco/3/GRCh38#130273078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105868069-C-A

130273108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105868060-T-C

130273219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105867946-G-A

http://identifiers.org/hco/3/GRCh38#130273243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105867922-C-A

130273243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105867922-C-T

http://identifiers.org/hco/3/GRCh38#130273267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#105867898-C-A

130273267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105867898-C-G

130273285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38501
most severe consequence: non coding transcript exon variant
orthologous variants: 105867880-T-C