143437730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626354-G-A

143437730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626354-G-T

http://identifiers.org/hco/8/GRCh38#143437772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75626396-C-A

143437802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626428-G-A

http://identifiers.org/hco/8/GRCh38#143437821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75626445-C-A

143437821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626445-C-T

143437863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626576-G-A

143437882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626591-G-A

143437882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626591-G-T

http://identifiers.org/hco/8/GRCh38#143437934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75626645-C-A

http://identifiers.org/hco/8/GRCh38#143437965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75626677-C-A

143437965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626677-C-T

143438001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3 prime UTR variant
orthologous variants: 75626712-C-T

143438074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: synonymous variant
orthologous variants: 75626786-G-A

http://identifiers.org/hco/8/GRCh38#143438106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75626816-A-C

http://identifiers.org/hco/8/GRCh38#143438126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75626833-C-A

143438138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75626852-C-T

143438158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75626872-G-A

143438158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75626872-G-T

143438180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75626893-C-G

143438180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75626893-C-T

143438184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75626897-G-C

143438632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75627340-G-A

143438632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75627340-G-C

143438712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75627395-C-T

143438740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75627418-C-T

143439132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75627819-T-C

143439132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75627819-T-G

143439683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75628370-T-C

http://identifiers.org/hco/8/GRCh38#143439979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75628464-C-A

143439979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75628464-C-G

143439979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75628464-C-T

http://identifiers.org/hco/8/GRCh38#143440227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75628664-A-C

143440227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense variant
orthologous variants: 75628664-A-G

http://identifiers.org/hco/8/GRCh38#143440334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75628786-C-A

http://identifiers.org/hco/8/GRCh38#143440445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75628891-C-A

143440445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75628891-C-T

http://identifiers.org/hco/8/GRCh38#143440462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75628915-C-A

143440496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75628964-G-T

http://identifiers.org/hco/8/GRCh38#143440643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75629126-C-A

143440728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629188-G-A

143440914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629367-A-G

143440914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629367-A-T

http://identifiers.org/hco/8/GRCh38#143441173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75629623-C-A

143441173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629623-C-G

143441173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629623-C-T

http://identifiers.org/hco/8/GRCh38#143441227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75629670-A-C

143441227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629670-A-G

143441231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629674-G-A

143441231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629674-G-T

143441397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75629797-C-T

143441754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75630172-C-T

143442080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75630533-G-A

143442157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75630625-G-A

143442223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75630694-G-A

143447004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75635615-G-A

143447018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75635629-G-A

143447102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75635706-G-C

143447341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75635914-G-A

143463938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75647122-T-C

143464199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75647389-C-T

143464376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75647579-C-T

143464377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75647580-G-A

143464415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75647628-G-A

143464415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75647628-G-C

143464667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75647920-G-A

143464904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75648116-G-A

143465031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75648234-G-A

143465072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75648278-A-T

143465294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75648477-T-C

http://identifiers.org/hco/8/GRCh38#143465298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75648481-C-A

143465298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75648481-C-T

http://identifiers.org/hco/8/GRCh38#143465301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75648484-C-A

143465570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75648723-G-T

http://identifiers.org/hco/8/GRCh38#143465604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75648755-C-A

143465646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75648797-T-G

143465993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649058-G-A

143465993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649058-G-T

143465996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649061-G-A

143465996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649061-G-T

143466038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649109-A-G

143466039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649110-G-A

143466089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649149-C-T

143466686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649595-T-C

143466687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649596-G-A

143466948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75649780-G-A

http://identifiers.org/hco/8/GRCh38#143467427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75650253-C-A

143467427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75650253-C-T

143467740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75650482-A-G

143467798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75650544-T-C

143467865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75650604-C-G

143468094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75650817-G-A

143468094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75650817-G-T

143468325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75651065-A-G

143468327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75651067-G-A

143468329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75651069-G-A

143468331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75651071-A-T

143468432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: synonymous variant
orthologous variants: 75651179-G-A

143468432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: synonymous variant
orthologous variants: 75651179-G-T

143468548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75651295-C-T

143468563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75651308-G-A

143468563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75651308-G-T

143469191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75651885-C-T

143470084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653307-G-A

143470301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653632-A-G

143470382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653709-G-A

143470396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653725-A-G

143470402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653731-G-A

143470402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653731-G-T

143470425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653744-C-T

143470483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653807-G-A

143470652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75653975-G-A

143471144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75654402-G-A

143471260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75654524-G-A

143471314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75654581-A-G

143471319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75654586-A-G

http://identifiers.org/hco/8/GRCh38#143471323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75654590-A-C

143471449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75654871-G-A

143471700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75655165-A-G

143474449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75656466-C-G

143474449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75656466-C-T

http://identifiers.org/hco/8/GRCh38#143474606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75656598-C-A

143474606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75656598-C-T

143474682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75656668-C-T

143475241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75657168-G-A

http://identifiers.org/hco/8/GRCh38#143475254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75657181-C-A

http://identifiers.org/hco/8/GRCh38#143475259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75657190-C-A

143475259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75657190-C-T

http://identifiers.org/hco/8/GRCh38#143475347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75657267-C-A

143476484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75658123-G-T

143476603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75658260-A-T

143476972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75658610-G-A

143477226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75658850-C-T

143477518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75659115-C-T

143477914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75659510-C-T

143478004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75659603-T-A

143478166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75659722-G-A

143478176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75659732-C-T

143478286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75659815-T-C

143478380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75659905-T-C

143478562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75659993-T-G

143478614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75660047-G-A

143478650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75660092-C-T

143478770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75660226-A-G

143479052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75660472-G-A

143479955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75661402-C-T

143482064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75662395-C-T

143482118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75662436-G-A

143482746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75662859-C-T

143483000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75663049-A-T

143483250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75663282-C-T

143484623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75664347-G-A

143484623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75664347-G-T

143484813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, missense_variant
orthologous variants: 75664557-T-C

http://identifiers.org/hco/8/GRCh38#143484854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75664594-C-A

143484854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 75664594-C-T

http://identifiers.org/hco/8/GRCh38#143484881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75664620-C-A

143484881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 75664620-C-T

143484942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, missense_variant
orthologous variants: 75664655-T-G

143485004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75664727-A-T

143485133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75664831-G-A

143485133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75664831-G-T

http://identifiers.org/hco/8/GRCh38#143485594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75665244-C-A

143485609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75665258-A-G

143485621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75665270-A-G

143485832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75665574-C-T

143485921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75665733-A-T

143485983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75665878-C-T

143485989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75665884-G-A

143486097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75666001-A-G

143486372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75666247-G-A

143486385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75666260-G-T

143486386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75666261-T-C

143486542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75666424-C-T

143486565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75666446-G-C

143486569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75666450-G-C

143489320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75667288-A-T

143490894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75668552-A-G

143490942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75668592-T-C

143491003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75668668-G-C

143491178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75668817-C-T

143491212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75668851-A-G

143491234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75668866-A-G

143491443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75669016-C-T

http://identifiers.org/hco/8/GRCh38#143491953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75669551-C-A

143491999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75669589-C-T

143492058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75669646-C-T

143492196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75669796-G-A

143492217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75669817-G-C

143493454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75670991-A-T

143494287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75671788-T-G

143494536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75671960-G-C

143494570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75671995-A-G

143494632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672056-G-C

143494632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672056-G-T

143494683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672098-C-G

143494707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672110-C-T

143494752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672141-G-C

143494941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672283-G-A

143494991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672353-G-A

143495014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672375-G-A

143495076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672439-C-T

143495077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75672440-G-A

143496148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75673021-T-A

143496193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, undefined
orthologous variants: 75673069-T-C

143496219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75673097-C-T

143496319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75673216-G-T

143496366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75673261-A-T

143496548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, undefined
orthologous variants: 75673448-T-A

143496579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75673486-G-A

143496630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75673538-G-A

143496669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75673578-G-C

143497252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75674117-G-A

143497825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75674467-G-A

143497825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75674467-G-C

143498111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75674780-G-A

143498165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75674861-G-A

143498257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75674952-T-A

143498264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75674959-C-T

143498483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75675154-G-A

143502305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75676919-G-A

143502305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75676919-G-T

143502868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75677483-G-A

http://identifiers.org/hco/8/GRCh38#143505034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75678871-C-A

http://identifiers.org/hco/8/GRCh38#143505374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75679197-C-A

143505607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75679442-G-A

143505622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75679457-C-T

143505969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75679740-A-T

http://identifiers.org/hco/8/GRCh38#143506079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75679868-C-A

143507016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75680713-C-T

143507080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75680777-C-T

143507186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75680865-C-G

143507186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75680865-C-T

143507234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75680898-T-C

143507234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75680898-T-G

143507364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75681010-G-A

143507364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75681010-G-T

143507680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75681311-G-A

143507688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron variant
orthologous variants: 75681319-G-T

143507778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: synonymous variant
orthologous variants: 75681409-G-A

143507778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: synonymous variant
orthologous variants: 75681409-G-T

143507924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681550-A-G

http://identifiers.org/hco/8/GRCh38#143507972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75681581-C-A

143507972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681581-C-T

http://identifiers.org/hco/8/GRCh38#143507981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75681590-C-A

143507981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681590-C-T

143507982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681591-T-C

143508107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681699-G-C

143508212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681805-C-T

http://identifiers.org/hco/8/GRCh38#143508375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75681906-C-A

143508375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75681906-C-T

143508696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75682212-C-T

143508759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75682230-A-G

143509270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75683708-A-G

143509412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683850-C-G

143509444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683878-T-C

143509482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75683906-C-T

143509567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684005-C-T

143509642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684075-C-T

143509646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684078-G-A

143509880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684208-G-A

143509986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684274-G-T

143510037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684318-A-T

http://identifiers.org/hco/8/GRCh38#143510392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75684630-C-A

143510401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684640-T-A

143510401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684640-T-C

143510413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75684652-G-A

http://identifiers.org/hco/8/GRCh38#143510669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75684878-C-A

143511191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685421-T-A

143511191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75685421-T-C

143511912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75686077-G-A

143511912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75686077-G-C

143511939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75686105-T-C

143512114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75686243-C-T

143512241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75686385-T-C

143512771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75687091-G-A

http://identifiers.org/hco/8/GRCh38#143513068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75687371-C-A

143513068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75687371-C-G

143513558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75688016-G-C

143513570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75688028-T-C

143513637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75688096-C-T

143514183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75688468-G-A

143514234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75688504-C-T

143514432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75688707-A-G

143515103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75689462-G-A

http://identifiers.org/hco/8/GRCh38#143515619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75689914-A-C

143515619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75689914-A-G

http://identifiers.org/hco/8/GRCh38#143516311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75690786-C-A

143516316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75690791-G-C

143516345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75690820-C-T

143516512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75690984-G-A

http://identifiers.org/hco/8/GRCh38#143516529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75690997-A-C

143516529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75690997-A-T

143516718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75691189-A-T

143516724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75691195-G-C

143516807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75691267-G-A

143517246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75691706-G-A

143517283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75691743-C-T

143518135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75692600-C-G

143518318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75692757-G-A

http://identifiers.org/hco/8/GRCh38#143518501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75692972-C-A

143518501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75692972-C-T

143518502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75692973-G-A

143518586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75693051-C-T

143518943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75693422-C-G

143518947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75693426-T-C

143519143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75693674-G-A

143524103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75694932-G-A

143524127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75694959-G-A

143524156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75695011-C-T

143524274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75695123-T-C

143524703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75695713-G-A

143524926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75695958-G-A

143525201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75696244-G-A

143525204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75696247-C-T

http://identifiers.org/hco/8/GRCh38#143525355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75696425-C-A

143525355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75696425-C-T

143525367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75696434-C-T

143525670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75696729-G-A

http://identifiers.org/hco/8/GRCh38#143527141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75701273-C-A

143527222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75701337-G-A

143527295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75701405-G-A

143527295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75701405-G-C

143527314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75701426-C-T

143527736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75701854-G-T

http://identifiers.org/hco/8/GRCh38#143527740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#75701858-A-C

143527841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75701958-C-G

143527848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75701965-G-C

143529479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75704502-C-T

143529486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75704510-G-A

143529531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75704566-C-T

143529573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75704616-C-T

143529771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75704840-G-A

143529888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75704960-C-G

143529934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75705010-C-T

143529988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75705068-C-T

143530121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75705185-T-C

143530195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75705246-C-T

143530236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75705276-G-A

143530236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75705276-G-C

143532324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75707569-A-G

143532332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75707577-G-A

143532332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75707577-G-C

143532469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75707677-T-C

143532840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708029-G-A

143532930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708111-C-T

143533070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708236-G-A

143533090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708277-C-T

143533220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708393-G-A

143533260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708426-G-A

143533260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708426-G-T

143533445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708592-C-T

143533450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75708598-T-C

143536205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75709269-T-A

143536205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75709269-T-C

143536324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75709383-C-T

http://identifiers.org/hco/8/GRCh38#143536516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75709579-C-A

143536516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75709579-C-T

http://identifiers.org/hco/8/GRCh38#143536987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75709959-A-C

143537012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75709970-G-A

143537012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75709970-G-C

143537172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710178-G-A

143537173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710179-T-G

143537304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710316-C-G

143537425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710431-G-A

143537434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710440-G-A

143537446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710452-G-C

143537779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710772-C-T

143537871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710883-C-G

143537871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710883-C-T

143537937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75710946-T-C

http://identifiers.org/hco/8/GRCh38#143537981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75711083-C-A

143537981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75711083-C-T

143538122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75711224-C-G

143538122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75711224-C-T

143538291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75711393-G-A

143538291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75711393-G-C

143538684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75711777-G-A

143538684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75711777-G-C

143538717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75711810-C-G

143538717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75711810-C-T

143538826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75711919-C-T

http://identifiers.org/hco/8/GRCh38#143539040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75712133-A-C

143539040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75712133-A-T

143539240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75712333-T-C

143539438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75712517-T-A

143539481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75712556-G-A

143539698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75712840-G-A

143539747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75712890-G-A

143539836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75712995-C-T

143541115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75713467-G-A

143541220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75713569-C-T

http://identifiers.org/hco/8/GRCh38#143541269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75713606-C-A

143541269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75713606-C-G

143541269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75713606-C-T

143541364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75713688-G-A

143541364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75713688-G-T

143541438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75713761-G-A

143541438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75713761-G-T