83968320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120173479-G-A

83968551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120173727-G-A

http://identifiers.org/hco/16/GRCh38#83968557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120173733-C-A

83968557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120173733-C-T

http://identifiers.org/hco/16/GRCh38#83968694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120173839-C-A

http://identifiers.org/hco/16/GRCh38#83968772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120173917-C-A

83968772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120173917-C-G

83968772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120173917-C-T

http://identifiers.org/hco/16/GRCh38#83968896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120174145-C-A

83968896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174145-C-T

83968898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174147-G-A

83968898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174147-G-C

83968898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174147-G-T

http://identifiers.org/hco/16/GRCh38#83968935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120174206-C-A

83968935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174206-C-T

83968971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174285-C-T

http://identifiers.org/hco/16/GRCh38#83968973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120174287-C-A

83968973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174287-C-G

83968973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174287-C-T

83969030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174447-C-G

83969224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174734-C-T

83969324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174824-C-G

83969393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174862-C-T

http://identifiers.org/hco/16/GRCh38#83969489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120174931-A-C

83969491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174933-T-A

83969702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175076-A-T

83969725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175096-G-T

83969995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175410-A-G

83970000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175415-C-G

http://identifiers.org/hco/16/GRCh38#83970018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120175419-C-A

83970018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175419-C-T

83970116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175480-C-G

83970140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175504-C-G

83970236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175613-C-G

http://identifiers.org/hco/16/GRCh38#83971315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120176070-C-A

83971315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176070-C-T

http://identifiers.org/hco/16/GRCh38#83971546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120176251-C-A

83971546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120176251-C-T

83971657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120176336-C-T

http://identifiers.org/hco/16/GRCh38#83971830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120176504-A-C

83971830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120176504-A-G

http://identifiers.org/hco/16/GRCh38#83972082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120176751-C-A

83972082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120176751-C-T

83972199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176867-G-A

83972199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176867-G-C

http://identifiers.org/hco/16/GRCh38#83972320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120176980-C-A

83972320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176980-C-G

83972321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176981-T-C

83973197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177176-C-T

83973218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177188-C-T

83973345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177280-G-C

83973445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177373-G-A

83973561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177469-A-G

83973715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177629-G-A

83973743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177657-C-T

83973779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177685-G-C

83973780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177686-G-T

83973782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177688-G-T

83975590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177723-G-C

83975609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177742-G-T

http://identifiers.org/hco/16/GRCh38#83975714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120177853-C-A

83975781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177911-A-G

83975840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177968-C-G

83976059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178152-G-A

http://identifiers.org/hco/16/GRCh38#83976132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120178222-C-A

83976205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178380-A-T

http://identifiers.org/hco/16/GRCh38#83978429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120178811-C-A

83978429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178811-C-T

83978448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120178825-T-C

83978469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120178846-A-G

83978578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178946-G-A

83978578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178946-G-T

83978598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178966-T-C

83978623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178988-G-T

83978640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179005-T-A

83978640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179005-T-C

83978656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179021-A-G

83978695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179069-T-C

83978820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179234-A-T

83979238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179543-C-T

http://identifiers.org/hco/16/GRCh38#83979275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120179576-C-A

83979275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179576-C-G

83979275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179576-C-T

http://identifiers.org/hco/16/GRCh38#83979336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120179633-C-A

83979336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179633-C-G

83979396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179689-A-G

83979758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179987-G-C

83979804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180028-G-T

83979827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180051-A-G

http://identifiers.org/hco/16/GRCh38#83979946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120180145-C-A

http://identifiers.org/hco/16/GRCh38#83979947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120180146-A-C

83980336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180365-C-G

83980354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180383-C-T

83980440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180455-C-T

83980593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180561-G-C

http://identifiers.org/hco/16/GRCh38#83980604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120180572-C-A

83980611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180579-C-T

83980619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180598-C-T

83980686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180753-C-G

83980775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180840-C-T

83980817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180900-C-G

83980817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180900-C-T

83980888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180989-C-T

83980895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180992-G-A

83980978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181042-G-A

http://identifiers.org/hco/16/GRCh38#83981191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120181275-C-A

83981191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181275-C-G

83981191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181275-C-T

http://identifiers.org/hco/16/GRCh38#83981255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120181312-C-A

83981255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181312-C-T

http://identifiers.org/hco/16/GRCh38#83981260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120181317-C-A

83981265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181322-T-C

83981269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181326-A-T

83981274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181330-C-G

http://identifiers.org/hco/16/GRCh38#83981337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120181407-A-C

83981364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181434-G-C

83981443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181491-T-C

83981443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181491-T-G

83987298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184822-G-T

83987341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184865-G-A

83987341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184865-G-C

83987357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184881-G-C

83987361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184885-C-G

83987361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184885-C-T

83988127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186740-G-A

83988217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186825-G-A

83988281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186890-C-T

83989372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188155-C-G

83989372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188155-C-T

83989523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188296-C-G

83989523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188296-C-T

http://identifiers.org/hco/16/GRCh38#83989531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120188304-A-C

83989540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188313-G-C

83989540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188313-G-T

83989548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188321-G-T

83989734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188459-A-G

83989736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188461-A-G

http://identifiers.org/hco/16/GRCh38#83989910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120188618-A-C

83990074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188837-C-T

83990459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189279-C-G

83990459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189279-C-T

http://identifiers.org/hco/16/GRCh38#83990468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120189288-C-A

83990468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189288-C-G

http://identifiers.org/hco/16/GRCh38#83990469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120189289-A-C

83990469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189289-A-G

http://identifiers.org/hco/16/GRCh38#83990520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120189326-C-A

83990520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120189326-C-G

83990520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120189326-C-T

83990639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189445-C-G

83990683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189459-C-T

83990814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189569-C-T

83990833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189585-A-G

http://identifiers.org/hco/16/GRCh38#83990838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120189590-A-C

http://identifiers.org/hco/16/GRCh38#83991951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120189690-C-A

83992138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189864-G-A

83992214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189928-T-G

83992230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189937-C-G

83992230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189937-C-T

83992239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189946-G-A

83992239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120189946-G-C

http://identifiers.org/hco/16/GRCh38#83992371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120190067-C-A

83992371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190067-C-G

83992371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190067-C-T

http://identifiers.org/hco/16/GRCh38#83992374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120190070-C-A

83992374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190070-C-G

http://identifiers.org/hco/16/GRCh38#83992387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120190083-C-A

83992387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190083-C-G

83992387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190083-C-T

83992475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190138-G-C

83992585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190228-G-A

http://identifiers.org/hco/16/GRCh38#83992628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120190271-C-A

83992628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190271-C-G

83992628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190271-C-T

83992670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190309-C-T

83992704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190326-G-A

83992713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190334-C-G

83992814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190378-G-A

83992875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120190432-C-T

83992938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190499-A-G

83992979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190540-G-C

83993115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190663-C-G

83993168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190716-G-A

83993191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190739-G-A

83993528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120191020-G-A

83993555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120191048-A-G

83993555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120191048-A-T

83993706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191132-A-G

83993734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191136-G-A

83993737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191139-C-G

83993737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191139-C-T

83993747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191149-G-C

83993747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191149-G-T

http://identifiers.org/hco/16/GRCh38#83993837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120191222-C-A

83993837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191222-C-G

83993837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191222-C-T

http://identifiers.org/hco/16/GRCh38#83993920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120191282-A-C

83993920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191282-A-T

83993973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120191344-C-G

83993973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120191344-C-T

83994041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191420-G-C

83994041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191420-G-T

83994108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191500-G-C

83994172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191540-G-T

83994249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191589-A-G

83994279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191619-G-A

83994331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120191670-C-T

http://identifiers.org/hco/16/GRCh38#83994356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120191695-C-A

83994470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191793-G-C

83994550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191843-C-T

http://identifiers.org/hco/16/GRCh38#83994554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120191847-C-A

83994554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191847-C-G

83994554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191847-C-T

83994641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120191924-G-A

83994641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120191924-G-T

http://identifiers.org/hco/16/GRCh38#83994725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120192006-A-C

83994725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192006-A-G

http://identifiers.org/hco/16/GRCh38#83994812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120192044-C-A

83994812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192044-C-T

http://identifiers.org/hco/16/GRCh38#83994831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120192062-C-A

83994831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192062-C-T

83995009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192172-G-C

83995096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192242-C-G

83995181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192299-C-G

83995181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192299-C-T

83995202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192321-T-C

83995205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192324-T-C

83995373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192445-T-G

83995480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192526-G-A

83995480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192526-G-T

83995663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192737-C-G

83995663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192737-C-T

83995772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192830-A-G

83995810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192883-G-C

83996119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193200-G-A

83996150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193232-G-A

83996185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193270-G-C

83996203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193279-C-T

83996257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193331-C-G

83996361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193407-C-T

http://identifiers.org/hco/16/GRCh38#83996386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120193431-C-A

83996386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193431-C-G

83996386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193431-C-T

83996393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193438-C-G

83996459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193485-G-C

83996498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193514-G-A

83996661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193649-G-A

83996661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193649-G-C

83996661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193649-G-T

http://identifiers.org/hco/16/GRCh38#83996824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120193802-C-A

83996824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193802-C-G

83996824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193802-C-T

83996834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193813-T-C

83996837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193816-A-T

http://identifiers.org/hco/16/GRCh38#83997094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120194150-C-A

83997094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194150-C-G

83997094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194150-C-T

83997176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194272-G-C

83997176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194272-G-T

83997189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194310-G-C

83997193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194314-C-G

83997193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194314-C-T

http://identifiers.org/hco/16/GRCh38#83997213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120194327-C-A

83997213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120194327-C-G

83997213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120194327-C-T

83997242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120194356-C-G

83997242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120194356-C-T

http://identifiers.org/hco/16/GRCh38#83997248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#120194362-A-C

83997248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 120194362-A-G

83997248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 120194362-A-T

http://identifiers.org/hco/16/GRCh38#83997327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120194431-C-A

83997327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194431-C-G

83997327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194431-C-T

83998094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194889-G-A

83998094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194889-G-T

83998119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194916-G-T

83998120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194917-G-A

83998120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194917-G-T

83998125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194922-G-A

83998125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194922-G-C

83998125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194922-G-T

http://identifiers.org/hco/16/GRCh38#83998198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120195001-C-A

83998198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120195001-C-G

83998198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120195001-C-T

83998249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120195052-A-G

83998339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195149-G-A

83998339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195149-G-C

83998376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195183-A-G

83998376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195183-A-T

83998388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195205-G-A

83998388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195205-G-C

83998388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195205-G-T

http://identifiers.org/hco/16/GRCh38#83998390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120195207-A-C

83998456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195253-T-C

84001738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198390-T-A

84001738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198390-T-G

84001747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198399-G-A

84001747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198399-G-C

84001747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198399-G-T

http://identifiers.org/hco/16/GRCh38#84001775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120198426-C-A

84001775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198426-C-G

84001775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198426-C-T

84001777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198428-G-A

84001777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198428-G-T

84001808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198462-A-G

http://identifiers.org/hco/16/GRCh38#84001817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120198471-C-A

84001817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120198471-C-G

84001817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120198471-C-T

84001891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120198545-G-A

84001891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120198545-G-C

84001897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120198551-C-G

84001897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120198551-C-T

84001923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120198577-G-A

84001923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120198577-G-C

84001923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120198577-G-T

84002097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198723-C-T

http://identifiers.org/hco/16/GRCh38#84002125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120198750-C-A

84002125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198750-C-T

84002193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198788-A-T

http://identifiers.org/hco/16/GRCh38#84002217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120198812-C-A

84002217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198812-C-G

84002217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198812-C-T

84002334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120198897-G-T

84002360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120198915-G-A

84002360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120198915-G-T

84002483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199041-T-G

http://identifiers.org/hco/16/GRCh38#84002577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120199126-C-A

84002577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199126-C-T

84002605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199159-G-A

84002605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199159-G-C

84002605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199159-G-T

84002617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199178-T-A

84002617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199178-T-C

84002617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199178-T-G

http://identifiers.org/hco/16/GRCh38#84002641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120199207-C-A

84002641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199207-C-G

84002641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199207-C-T

84002650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199220-C-T

http://identifiers.org/hco/16/GRCh38#84002688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120199268-A-C

84002688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199268-A-G

84002688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23746
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120199268-A-T