108822816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 48592392-G-A

108822940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48592269-T-A

108822949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48592260-A-T

108822956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48592253-T-G

108823082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48592107-A-T

http://identifiers.org/hco/3/GRCh38#108823083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48592106-A-C

108823083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48592106-A-G

108823083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48592106-A-T

108823101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48592090-G-A

108823314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48591878-T-G

108823356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48591814-G-T

108823450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48591757-G-C

108824207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48591342-A-G

108824339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48591210-T-G

108824601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590949-T-G

108824668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590874-T-C

108825128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590644-T-C

108825318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590584-A-G

108825428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590464-A-G

108825428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590464-A-T

108825526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590387-G-A

108825529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590384-T-A

108825658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48590243-C-T

108825957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589969-T-C

108825964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589962-C-T

108826200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589718-C-G

108826450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589444-T-C

108826598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589295-C-T

108826711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589175-C-T

108826760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589123-A-G

108826826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589066-T-C

108826887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48589007-A-T

108826930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588964-G-T

108827188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588710-T-C

108827189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588709-A-G

108827382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588566-G-A

108827382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588566-G-C

108827384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588564-A-G

108827424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588500-G-A

108827489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588386-A-G

108827516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588359-G-A

108827517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588358-G-A

108827684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588210-A-T

http://identifiers.org/hco/3/GRCh38#108827760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48588129-A-C

108827857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48588034-T-C

108828648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48586797-G-A

108828892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48586571-G-A

108828995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48586472-C-T

108829152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48586323-T-C

108829162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48586313-T-A

108829164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48586311-C-T

108830134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48582465-A-G

108830219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48582380-A-G

108830219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48582380-A-T

108830337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48582289-A-G

108830450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48582180-T-C

108830494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48582141-T-C

108830593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48581910-T-G

http://identifiers.org/hco/3/GRCh38#108830805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48581700-A-C

108830805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48581700-A-G

http://identifiers.org/hco/3/GRCh38#108830843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48581672-A-C

108830852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48581663-G-A

108830852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48581663-G-C

108830852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48581663-G-T

http://identifiers.org/hco/3/GRCh38#108830882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48581634-A-C

108830882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48581634-A-G

108830882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48581634-A-T

http://identifiers.org/hco/3/GRCh38#108831383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48581219-C-A

108831383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48581219-C-G

108833514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48580651-T-C

108833645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48580521-T-C

108833833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48580345-T-C

http://identifiers.org/hco/3/GRCh38#108833868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48580313-C-A

108833868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48580313-C-G

108833884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48580297-C-T

108833951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48580208-T-C

108834125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48580048-T-C

108834145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48580036-A-G

108834277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579907-A-G

108834293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579901-G-T

108834365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579809-C-T

108834366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579808-C-T

108834390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579795-C-G

108834444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579744-C-T

108834665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579543-T-A

108835014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579201-T-A

108835186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48579011-G-A

108835323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48578879-G-A

http://identifiers.org/hco/3/GRCh38#108835554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48578696-C-A

http://identifiers.org/hco/3/GRCh38#108835686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48578556-C-A

http://identifiers.org/hco/3/GRCh38#108835809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48578416-A-C

108836873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576909-T-C

108836900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576873-A-G

108836949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576819-G-A

108837017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576751-T-C

108837064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576714-C-T

108837130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576641-T-C

108837277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576497-T-C

108837283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576491-T-C

108837328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576446-T-C

108837667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576126-T-C

http://identifiers.org/hco/3/GRCh38#108837753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48576043-A-C

108837753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576043-A-T

108837768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48576028-G-A

http://identifiers.org/hco/3/GRCh38#108838195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48575641-C-A

108838201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575635-A-G

108838247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575614-A-G

108838273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575593-T-C

108838387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575492-T-C

108838479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575406-T-A

108838487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575398-G-A

108838519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575366-A-T

108838575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575313-G-A

108838699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48575170-C-G

108838810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48574754-T-A

108838810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48574754-T-C

108838836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48574728-T-A

108838836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48574728-T-C

108838973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574604-T-A

108838973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574604-T-C

108839023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574554-A-G

http://identifiers.org/hco/3/GRCh38#108839047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48574530-C-A

108839047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574530-C-T

108839111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574465-T-C

http://identifiers.org/hco/3/GRCh38#108839112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48574464-C-A

108839197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574382-T-C

108839197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574382-T-G

108839227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574352-T-A

108839227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574352-T-C

108839227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574352-T-G

108839236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574342-T-A

108839236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574342-T-C

108839257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574307-T-A

108839257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574307-T-C

108839257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48574307-T-G

108839585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48572646-G-T

108839639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48572588-T-C

108839678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48572539-T-A

http://identifiers.org/hco/3/GRCh38#108839688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48572529-C-A

108839833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48572302-T-C

108839861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48572282-A-G

108839861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48572282-A-T

108839990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48572162-T-C

108840088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571992-G-C

108840203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571885-A-G

108840269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571829-A-T

108840474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571518-G-A

http://identifiers.org/hco/3/GRCh38#108840531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48571461-C-A

108840557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571435-T-A

108840557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571435-T-C

108840791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571200-A-G

108840860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571127-C-T

108840945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48571050-A-G

108841321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48568050-T-C

108841504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48567889-G-A

http://identifiers.org/hco/3/GRCh38#108841754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48567657-A-C

108843975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48565302-G-A

108844091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48565183-A-G

http://identifiers.org/hco/3/GRCh38#108844118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48565156-C-A

108844882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48564878-T-A

108844954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48564810-G-A

108844990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48564774-A-G

108845128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48564531-C-T

108845486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48564171-A-G

108845514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48564151-A-G

http://identifiers.org/hco/3/GRCh38#108845805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48563867-C-A

108846102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48563591-A-G

108846131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48563562-G-A

108846221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48563468-G-A

http://identifiers.org/hco/3/GRCh38#108846499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48563285-A-C

108846499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48563285-A-G

108846590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48563190-G-A

108846613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48563174-G-A

108846853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48562904-A-G

108846957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48562782-G-A

108846957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48562782-G-T

108846975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48562764-T-A

108847105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48562584-G-A

108847105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48562584-G-T

108847108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48562581-A-G

108847108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48562581-A-T

108847171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48562517-A-G

108847217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48562480-T-C

108847305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48562403-T-C

108847355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48562351-T-G

108847377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48562310-G-A

108847377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48562310-G-C

http://identifiers.org/hco/3/GRCh38#108847418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48562273-C-A

108847418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48562273-C-T

108847591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48562086-G-A

108847755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48561954-G-A

108847890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48561830-A-G

108847913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48561808-A-G

http://identifiers.org/hco/3/GRCh38#108848143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48561595-A-C

http://identifiers.org/hco/3/GRCh38#108848572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48561237-C-A

108848630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48561174-G-A

108848655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48561153-G-A

108848795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48561006-A-G

108848888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48560898-C-G

108848888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48560898-C-T

108848938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48560849-A-G

108849222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense variant
orthologous variants: 48560570-A-T

108849227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense variant
orthologous variants: 48560565-G-T

108849247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense variant
orthologous variants: 48560545-C-G

http://identifiers.org/hco/3/GRCh38#108849269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48560509-C-A

108849269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48560509-C-T

108849300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48560473-A-G

108849315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48560461-T-A

108849393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48560384-G-C

108849393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48560384-G-T

108850242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48559913-C-G

108850263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48559892-T-A

108850263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48559892-T-C

108850263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48559892-T-G

108850752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48559159-C-T

108850753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48559158-A-G

http://identifiers.org/hco/3/GRCh38#108850851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48559042-A-C

108851451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48558465-C-T

108851479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48558434-C-T

http://identifiers.org/hco/3/GRCh38#108851805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48558099-A-C

108851841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48558066-A-G

http://identifiers.org/hco/3/GRCh38#108852543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48556524-A-C

108852550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48556517-T-A

108852659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48556424-T-C

108853101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48555900-A-G

108853107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48555894-T-C

108853471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48555551-G-A

108853471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48555551-G-T

108853544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48555485-C-T

108853608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: intron variant
orthologous variants: 48555417-C-T

108853623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense variant
orthologous variants: 48555389-A-G

108853682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: synonymous variant
orthologous variants: 48555330-A-G

http://identifiers.org/hco/3/GRCh38#108853705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48555307-A-C

108853705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense variant
orthologous variants: 48555307-A-T

108853723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense variant
orthologous variants: 48555289-G-A

108853728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: missense variant
orthologous variants: 48555284-G-A

108853728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: stop gained
orthologous variants: 48555284-G-T

http://identifiers.org/hco/3/GRCh38#108853976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48555051-A-C

108854043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: 48554984-A-G

http://identifiers.org/hco/3/GRCh38#108854071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48554960-C-A

108854071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: 48554960-C-T

108854238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: 48554828-G-A

108854238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: 48554828-G-T

108854361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: 48554685-A-G

108854365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: 48554681-T-G

http://identifiers.org/hco/3/GRCh38#108854580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48554459-C-A

108854603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: 48554434-G-T

http://identifiers.org/hco/3/GRCh38#108854650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48554391-C-A

108854650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: 48554391-C-T

http://identifiers.org/hco/3/GRCh38#108854759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30698
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48554200-C-A