130070591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 30401939-T-C

130070616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 30401965-A-G

130070619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 30401968-G-A

130070619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 30401968-G-C

130070619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 30401968-G-T

http://identifiers.org/hco/7/GRCh38#130070724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#30402073-C-A

130070724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 30402073-C-G

130070724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 30402073-C-T

130070945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30402242-G-A

130070945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30402242-G-T

130071109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30402403-C-G

130071498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30402821-A-G

130071629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30402931-A-G

130072221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, undefined
orthologous variants: 30403536-C-T

http://identifiers.org/hco/7/GRCh38#130072602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30403947-C-A

130072602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30403947-C-T

http://identifiers.org/hco/7/GRCh38#130072672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30404012-A-C

130074524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30405699-A-G

130074652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30405802-G-T

130075052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30406154-T-A

130075052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30406154-T-G

130087633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30412793-G-A

130087685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30412845-A-G

130087797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30412915-G-T

130087922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30413029-G-A

130092197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30422897-G-T

130092474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30423159-C-T

130092703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30423385-T-C

130092769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30423451-T-C

130092790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30423470-G-A

130092933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30423615-T-C

130092950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30423643-T-G

130093155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30423859-T-C

130093226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30423947-A-T

130093364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30424073-C-G

130093364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30424073-C-T

130093721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30424467-T-C

130093986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30424706-C-T

130094298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30424977-A-G

130094345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30425024-C-G

130094614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30425274-T-C

130094959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30425612-A-G

130095157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30425814-T-C

130096047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30426545-G-A

130096192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30426672-A-G

130096381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30426864-C-T

130096420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30426933-A-G

130096629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30427437-A-G

130096629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30427437-A-T

130096659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30427460-C-T

130096704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30427500-T-C

130097061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30427848-G-A

130097061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30427848-G-C

130097061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30427848-G-T

130097831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30428709-T-C

130098038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30429018-C-T

http://identifiers.org/hco/7/GRCh38#130098190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30429226-A-C

130098353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30429299-C-T

130098453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30429382-A-G

130098713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30429642-G-A

130098883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30430588-G-C

130098884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30430589-C-G

130098977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30430679-G-A

130099147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30430870-C-T

130099172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30430893-C-T

130099303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30431005-T-C

http://identifiers.org/hco/7/GRCh38#130099383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30431094-A-C

130099410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30431120-A-G

130099590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30431277-A-T

130099717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30431387-G-A

130099717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30431387-G-C

http://identifiers.org/hco/7/GRCh38#130099722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30431392-C-A

130100511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30432136-T-C

http://identifiers.org/hco/7/GRCh38#130112151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30435273-C-A

130112161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30435283-A-G

130112417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30435614-C-T

130112472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30435730-C-T

130112764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30436109-G-A

130112882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30436216-G-A

130113069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30436368-A-G

http://identifiers.org/hco/7/GRCh38#130113567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30436700-A-C

130113567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30436700-A-G

130113571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30436705-C-G

130113599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30436730-C-T

130113740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30436856-C-T

130114284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30437431-C-G

130114312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30437460-G-A

130114833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30437955-G-A

130115129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30438244-C-G

130115199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30438321-A-T

130115393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30438501-C-T

http://identifiers.org/hco/7/GRCh38#130115497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30438682-C-A

130115559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30438741-C-T

130115935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439182-G-A

130115937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439184-A-G

130116011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439229-G-A

130116088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439291-A-G

130116351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439552-G-A

130116351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439552-G-T

http://identifiers.org/hco/7/GRCh38#130116353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30439554-C-A

130116353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439554-C-T

130116364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439565-G-A

130116364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439565-G-T

130116389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439589-G-A

http://identifiers.org/hco/7/GRCh38#130116415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30439613-C-A

130116416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30439614-C-T

130116442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 30439640-T-G

130116605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30439803-A-G

130116704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439902-A-G

130116750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439949-T-G

130116773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439972-G-A

130116773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439972-G-C

130116773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439972-G-T

130116814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440015-A-G

130116835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440036-G-A

130116979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440200-T-G

130120063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30441346-G-T

http://identifiers.org/hco/7/GRCh38#130120658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30441685-A-C

130120679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30441707-T-G

130120689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30441717-A-G

130120689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30441717-A-T

130120798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: synonymous variant
orthologous variants: 30441825-A-G

130121039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30442067-T-G

130121150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30442481-G-A

130121239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30442545-G-A

130121621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30442885-A-G

130121656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30442909-G-A

130121656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30442909-G-C

http://identifiers.org/hco/7/GRCh38#130122024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30444404-C-A

130122024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30444404-C-G

130122024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30444404-C-T

130122227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30444595-T-G

130122396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30444723-C-T

130124044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30446198-A-G

http://identifiers.org/hco/7/GRCh38#130124057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30446210-C-A

130124084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30446235-G-T

http://identifiers.org/hco/7/GRCh38#130124350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30446511-C-A

130124350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30446511-C-T

130124555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30446722-A-G

130124584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30446749-A-G

130124588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30446753-T-C

http://identifiers.org/hco/7/GRCh38#130124599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30446765-A-C

130124931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30447019-G-A

130125746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30447300-T-C

130125785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30447332-A-G

130125854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30447398-T-G

130125977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30447519-A-G

130125998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30447536-G-A

130125998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30447536-G-T

130127802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30448301-T-G

130127866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30448363-G-C

130128563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30448979-C-T

130129178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30449331-T-G

130129357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30449432-G-A

130129357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30449432-G-T

130129594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30449645-T-A

130129782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30449767-G-A

130129947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30449863-C-G

130130085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30449969-G-C

http://identifiers.org/hco/7/GRCh38#130130126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30450034-C-A

130130126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450034-C-T

130130131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450039-A-G

130130144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450051-C-T

http://identifiers.org/hco/7/GRCh38#130130303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30450189-C-A

http://identifiers.org/hco/7/GRCh38#130130312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30450198-A-C

130130355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450245-G-A

130130355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450245-G-T

130130385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450275-A-T

130130404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450294-A-G

130130445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450379-T-C

130130476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: intron variant
orthologous variants: 30450418-G-A

130130539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 30450488-T-C

130130635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: synonymous variant
orthologous variants: 30450584-G-C

130130731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: synonymous variant
orthologous variants: 30450680-C-T

130130829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30450778-A-G

130131019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30450963-G-T

http://identifiers.org/hco/7/GRCh38#130131263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30451200-A-C

130131263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451200-A-G

130131263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451200-A-T

130131354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451263-G-T

130131411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451315-G-A

130131411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451315-G-T

130131418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451321-G-T

130131554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451424-T-C

130131656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451521-G-T

130132120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451933-G-A

130132167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 30451979-C-T

130132182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451994-G-A

130132182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30451994-G-T

130132206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 30452018-G-T

130132309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452118-A-G

130132398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452207-G-A

130132398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452207-G-T

http://identifiers.org/hco/7/GRCh38#130132457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30452252-C-A

130132593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452340-G-T

http://identifiers.org/hco/7/GRCh38#130132614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30452361-C-A

130132779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452513-G-T

130132838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452572-T-A

130132838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452572-T-C

130133073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452795-A-G

130133073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452795-A-T

http://identifiers.org/hco/7/GRCh38#130133136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30452848-C-A

130133136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452848-C-T

130133140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30452853-A-G

130133344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30453051-T-A

130133344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30453051-T-C

130133423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30453129-G-T

130133555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30453253-G-T

130133830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30453507-C-T

http://identifiers.org/hco/7/GRCh38#130133893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30453569-C-A

130134096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30453782-A-G

http://identifiers.org/hco/7/GRCh38#130134387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30454012-C-A

130134387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454012-C-G

130134398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454023-G-A

130134398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454023-G-C

130134398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454023-G-T

130134442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454065-G-A

130134442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454065-G-T

130134455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454078-C-T

130134456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454079-G-T

130134501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454124-G-T

130134669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454281-G-A

130134669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454281-G-T

130135317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454830-G-A

130135317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22194
most severe consequence: 3 prime UTR variant
orthologous variants: 30454830-G-T