23061476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121241316-G-A

http://identifiers.org/hco/16/GRCh38#23061604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121241445-C-A

23061728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121241559-C-G

23061908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121241767-C-T

23062030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121241856-T-C

http://identifiers.org/hco/16/GRCh38#23062123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121241937-A-C

23062184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121241993-G-A

23062184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121241993-G-C

http://identifiers.org/hco/16/GRCh38#23062361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121242147-C-A

23062364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242150-T-A

23062499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242263-G-A

23062585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242323-G-T

23062607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242348-C-G

23062607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242348-C-T

23062785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242530-T-A

23062785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242530-T-C

23062850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242646-T-C

23062964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242758-T-G

23062997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121242780-A-G

23063281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243001-T-C

23063281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243001-T-G

http://identifiers.org/hco/16/GRCh38#23063285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121243005-C-A

23063285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243005-C-G

23063285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243005-C-T

http://identifiers.org/hco/16/GRCh38#23063378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121243098-A-C

http://identifiers.org/hco/16/GRCh38#23063439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121243158-C-A

23063445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243164-A-G

23063560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243277-T-C

23063613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243337-A-G

23063761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243484-T-G

23064121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243848-G-A

23064273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121243982-T-C

23064357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244052-T-C

23064495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244188-C-G

23064496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244189-G-A

23064496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244189-G-T

http://identifiers.org/hco/16/GRCh38#23064527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121244218-C-A

23064662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244295-A-G

http://identifiers.org/hco/16/GRCh38#23064682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121244313-C-A

23064682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244313-C-T

23065086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244651-A-G

23065164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244741-C-T

23065168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244744-A-G

23065189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121244765-C-T

http://identifiers.org/hco/16/GRCh38#23066072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121245536-C-A

23066072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245536-C-T

23066103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245571-G-A

23066103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245571-G-C

23066103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245571-G-T

23066195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245658-C-T

23066272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245736-T-C

23066279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245743-G-A

23066344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245789-G-A

23066344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245789-G-T

23066529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121245947-T-A

23066765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121246149-G-A

23067177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121246557-G-A

23067240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121246622-A-G

23067388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121246760-G-A

23067395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121246767-T-C

23067414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121246779-G-A

http://identifiers.org/hco/16/GRCh38#23067603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121246983-C-A

23067603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121246983-C-T

http://identifiers.org/hco/16/GRCh38#23067635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121247015-C-A

23067687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121247064-T-A

http://identifiers.org/hco/16/GRCh38#23067747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121247124-A-C

23067992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121247355-G-C

23067992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121247355-G-T

23068131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121247492-C-T

23068151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121247512-A-G

23068634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121247995-C-G

23068634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121247995-C-T

23068721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121248082-T-C

http://identifiers.org/hco/16/GRCh38#23068884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121248242-C-A

23068884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121248242-C-T

23068940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121248298-A-T

23068977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121248335-C-T

23068985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121248343-C-G

23068985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121248343-C-T

23068986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121248344-C-T

23069018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121248376-G-C

23069597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121248955-T-C

23069717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121249064-G-A

23069717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121249064-G-C

23069825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121249173-C-T

23070043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121249350-T-C

http://identifiers.org/hco/16/GRCh38#23070211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121249496-C-A

23070776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121249650-C-T

23070789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121249661-C-G

23071170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121250017-A-G

23071840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121250586-C-T

http://identifiers.org/hco/16/GRCh38#23071894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121250604-A-C

23071894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121250604-A-G

23071934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121250631-T-C

http://identifiers.org/hco/16/GRCh38#23072014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121250674-C-A

23072014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121250674-C-T

23072055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121250715-A-G

23072076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121250736-C-T

23072193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121250853-G-T

23072208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 121250868-G-A

23072208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 121250868-G-C

23072208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 121250868-G-T

23072233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121250892-G-A

23072233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121250892-G-C

23072233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121250892-G-T

23072378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121251006-G-T

23072582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121251189-T-C

23072620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121251223-T-A

23072620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121251223-T-C

23072677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121251294-C-T

23072714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121251353-C-G

23072800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121251429-C-T

23073074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121251719-G-A

http://identifiers.org/hco/16/GRCh38#23073137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#121251749-C-A

23073334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121251943-A-G

23073363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121251973-T-C

23073840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121252443-G-A

23074001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252602-G-T

23074025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252647-A-T

23074029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252651-T-C

http://identifiers.org/hco/16/GRCh38#23074030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121252652-C-A

23074089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252711-G-A

23074089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252711-G-T

23074228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252830-G-A

23074230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252832-G-A

23074230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252832-G-T

23074300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252890-G-A

23074300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121252890-G-C

23074713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121253531-G-A

23074784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121253623-G-A

23074813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121253716-T-A

23074877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121253781-A-G

23075007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121253904-C-T

23075086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121253968-C-T

23075087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121253969-C-G

23075087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121253969-C-T

23075270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121254103-A-G

http://identifiers.org/hco/16/GRCh38#23075485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121254471-A-C

23075966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121255002-T-C

23075966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121255002-T-G

23075993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121255056-T-A

23076004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121255067-T-C

23076434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121255505-A-T

23076488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121255555-G-C

23076636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121255662-A-G

http://identifiers.org/hco/16/GRCh38#23076848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121255846-C-A

23076848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121255846-C-G

23077153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121256104-A-G

23077450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121256322-A-G

23077454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121256326-T-C

23077630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121256504-G-A

23078168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121256821-T-C

23078494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121257008-C-T

23078511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121257026-C-G

23078605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121257096-G-A

23078713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121257190-C-T

23078926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121257329-G-C

http://identifiers.org/hco/16/GRCh38#23078965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121257369-C-A

23078965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121257369-C-G

23079003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257410-T-C

23079036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257442-G-A

23079070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257475-T-C

23079096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257494-A-G

23079327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257716-G-T

23079605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257801-G-A

23079605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257801-G-C

23079605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257801-G-T

23079653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257843-G-A

23079653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257843-G-T

23079690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257877-T-C

http://identifiers.org/hco/16/GRCh38#23079724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121257898-C-A

23079724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257898-C-G

23079724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121257898-C-T

http://identifiers.org/hco/16/GRCh38#23079753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121257928-C-A

23079782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121257954-T-C

23079782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121257954-T-G

23079815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121257986-G-A

23079882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121258048-T-C

23079882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121258048-T-G

23079911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121258076-G-A

23079911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121258076-G-T

23080284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121258449-G-A

23080284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121258449-G-T

23080339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121258496-A-G

23080587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121258741-T-G

http://identifiers.org/hco/16/GRCh38#23080913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121259043-C-A

23080980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121259108-A-G

http://identifiers.org/hco/16/GRCh38#23080995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121259116-A-C

23081085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121259201-T-C

23081161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121259289-A-G

23081242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121259344-C-T

23081243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121259345-C-G

23081444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121259585-C-T

23081749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121259852-G-A

23081992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121260079-C-G

http://identifiers.org/hco/16/GRCh38#23082365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121260501-C-A

23082365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121260501-C-T

23082403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121260537-A-T

23082425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121260556-A-G

23082536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121260667-G-A

23082599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121260731-C-G

23082599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121260731-C-T

23083258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121263020-G-C

23083264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121263026-C-G

23083264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121263026-C-T

http://identifiers.org/hco/16/GRCh38#23083658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121263367-C-A

23083658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121263367-C-T

23083941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121263571-T-C

23084009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121263625-T-C

23084268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121265015-T-A

23084270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121265017-C-T

http://identifiers.org/hco/16/GRCh38#23084322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121265068-C-A

23084322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121265068-C-T

23084356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121265123-A-G

23084357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121265124-C-T

23084745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121265957-T-C

23084962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121266129-A-G

23085029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121266195-G-A

23085054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121266219-A-T

http://identifiers.org/hco/16/GRCh38#23085085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121266250-C-A

23085085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121266250-C-G

http://identifiers.org/hco/16/GRCh38#23085194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121266340-C-A

23085264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121266622-A-G

23085353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121266768-T-C

23085471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121266881-T-A

23085539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121266944-T-A

23085539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121266944-T-C

23085688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121267104-G-A

23086180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121267553-T-C

23086204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121267578-T-A

23086204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121267578-T-C

23086395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121267842-T-G

23086605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121268275-G-A

23087009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121268799-G-T

http://identifiers.org/hco/16/GRCh38#23087026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121268823-C-A

23087067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121268856-T-A

23087070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121268859-T-C

http://identifiers.org/hco/16/GRCh38#23087229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121269013-A-C

23087229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121269013-A-G

23087271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121269053-G-A

http://identifiers.org/hco/16/GRCh38#23087276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121269058-A-C

23087276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121269058-A-G

23087276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121269058-A-T

http://identifiers.org/hco/16/GRCh38#23087294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121269076-C-A

23087372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121269118-T-A

23087583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121269305-G-T

23087667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121269382-T-A

23088180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121269817-G-A

23088789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270815-T-C

23088818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270843-T-C

http://identifiers.org/hco/16/GRCh38#23088947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121270973-A-C

23088969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270995-C-T

23089630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271563-A-G

23089978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271891-T-C

http://identifiers.org/hco/16/GRCh38#23089991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121271904-A-C

23090263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272112-A-G

23090596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272273-A-G

23090596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272273-A-T

23090598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272275-T-A

http://identifiers.org/hco/16/GRCh38#23090746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121272419-C-A

23090746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121272419-C-T

23090749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121272422-T-G

23090752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121272425-A-G

23090875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272563-T-A

23090875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272563-T-C

http://identifiers.org/hco/16/GRCh38#23090882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121272570-C-A

23090882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272570-C-T

23091019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272701-C-G

23091019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272701-C-T

23091207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272893-A-G

23102212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273984-A-G

23102232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274002-T-A

23102232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274002-T-C

http://identifiers.org/hco/16/GRCh38#23102284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121274048-C-A

23102284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274048-C-G

23102303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274065-A-G

23102471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121274231-T-C

23102471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121274231-T-G

http://identifiers.org/hco/16/GRCh38#23102547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121274311-C-A

23102557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274320-G-A

23102557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274320-G-T

23102579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274342-C-T

http://identifiers.org/hco/16/GRCh38#23103221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121274623-A-C

23103229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274631-T-C

23103590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275002-T-C

23103964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275029-C-T

23103978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275043-G-A

http://identifiers.org/hco/16/GRCh38#23104497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121275554-A-C

23104604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121275651-T-C

23104820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275841-G-A

23105008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276100-A-G

23105292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276308-G-A

23105292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276308-G-C

23105292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276308-G-T

23105329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276355-G-T

23105358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276379-G-A

23105358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276379-G-T

23105395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276419-A-T

23105546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121276570-G-C

23105630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276654-T-A

23105630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276654-T-C

http://identifiers.org/hco/16/GRCh38#23105682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121276707-C-A

http://identifiers.org/hco/16/GRCh38#23106087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121277210-C-A

http://identifiers.org/hco/16/GRCh38#23106150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121277270-C-A

23106232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121277349-T-C

23106489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 121277605-T-A

23106489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 121277605-T-C

http://identifiers.org/hco/16/GRCh38#23106570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121277684-C-A

http://identifiers.org/hco/16/GRCh38#23106588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121277702-C-A

23106614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277727-T-C

23107227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277910-C-T

23107426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278089-A-G

23107576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278217-T-G

http://identifiers.org/hco/16/GRCh38#23107617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121278259-A-C

http://identifiers.org/hco/16/GRCh38#23107916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121278473-C-A

23107916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278473-C-T

23108003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278567-T-A

http://identifiers.org/hco/16/GRCh38#23108004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121278568-C-A

http://identifiers.org/hco/16/GRCh38#23108037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121278601-C-A

23108037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278601-C-G

23108037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278601-C-T

23108142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121278704-G-A

23108163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121278725-T-C

23108163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121278725-T-G

http://identifiers.org/hco/16/GRCh38#23108203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121278762-A-C

23108212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278771-A-T

23108274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278825-T-A

23110542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279141-G-A

23110851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279376-G-A

23111207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279392-T-A

23111210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279395-T-A

23111210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279395-T-C

23111315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279492-G-A

23111463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279609-G-A

23111463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279609-G-C

23111619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279755-T-G

23111653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279783-T-C

23111755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121279888-T-C

23112443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121280559-C-G

http://identifiers.org/hco/16/GRCh38#23113591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121281314-C-A

23114030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121281457-G-A

23114220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121281576-G-A

23114388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121281768-G-A

http://identifiers.org/hco/16/GRCh38#23114515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121281849-C-A

http://identifiers.org/hco/16/GRCh38#23114550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121281881-C-A

23114550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121281881-C-T

23114740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121282068-C-G

http://identifiers.org/hco/16/GRCh38#23114790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121282118-A-C

23114790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121282118-A-G

23114826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121282153-A-G

23114834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121282160-T-A

23114969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121282307-T-C

23115373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121282659-G-A

23115564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121282875-A-G

http://identifiers.org/hco/16/GRCh38#23115732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121283008-C-A

23115767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283035-G-A

http://identifiers.org/hco/16/GRCh38#23115828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121283083-C-A

23115828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283083-C-T

23116104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283378-A-G

23116174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283439-C-G

23119477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285637-C-T

23119506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285668-T-G

23119507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285669-C-G

23119903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121289736-T-C

http://identifiers.org/hco/16/GRCh38#23119998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121289811-C-A

http://identifiers.org/hco/16/GRCh38#23120317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121290136-A-C

23120430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290260-T-A

23120430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290260-T-C

23120438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290268-T-C

23120551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290325-G-A

23120716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290562-G-A

23121067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291057-A-T

23121074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291064-A-G

23121208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291198-T-C

23121247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291227-G-A

23121411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291373-C-G

http://identifiers.org/hco/16/GRCh38#23121480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121291439-C-A

23121480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291439-C-G

23121811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291777-T-C

23121836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291788-G-A

23122169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292068-C-T

23122249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292122-A-G

23122392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292187-A-G

23122474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292243-C-G

23122481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292250-A-G

23122481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292250-A-T

23122591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292388-A-T

23122690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292483-A-G

http://identifiers.org/hco/16/GRCh38#23122755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121292553-C-A

23122974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292949-T-C

23122986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292964-A-G

23123202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293132-G-A

23129580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293911-T-C

23129586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293917-T-C

23129623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293954-G-A

23130080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121294521-T-C

23130222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121294635-T-C

23130775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295024-T-A

23130775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295024-T-C

23130801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295044-A-G

23131472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295243-G-A

23131880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121296415-C-G

23131880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121296415-C-T

23132554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297104-C-T

23132591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297140-T-C

23132591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297140-T-G

http://identifiers.org/hco/16/GRCh38#23132667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121297400-A-C

23132838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297548-A-G

23132954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297661-T-C

23133563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298181-T-C

23133614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298231-C-T

23134142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298412-G-T

http://identifiers.org/hco/16/GRCh38#23134628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121298834-C-A

23134709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298880-T-A

23134977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298897-G-A

23135018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298938-C-T

23135040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298965-C-T

23135041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298966-G-A

23135041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298966-G-T

http://identifiers.org/hco/16/GRCh38#23135395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121299255-A-C

23135395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299255-A-G

http://identifiers.org/hco/16/GRCh38#23135625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121299581-C-A

23135665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299616-T-A

23135665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299616-T-C

23135943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299880-T-A

23135945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299882-C-G

23141067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300075-A-G

23141068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300076-C-T

http://identifiers.org/hco/16/GRCh38#23141096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121300104-C-A

23141096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300104-C-G

23141323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300304-T-C

23141323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300304-T-G

http://identifiers.org/hco/16/GRCh38#23142386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121301378-A-C

http://identifiers.org/hco/16/GRCh38#23142456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121301453-C-A

23142515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301512-G-T

23143915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302195-C-T

23144455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302726-C-T

23144887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302802-G-A

http://identifiers.org/hco/16/GRCh38#23145016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121302914-A-C

23145016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302914-A-G

23145096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302997-C-G

23145096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302997-C-T

23145239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121303123-C-T

23145374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121303264-A-G

23145397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121303284-G-A

23145578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121303494-A-T

23146083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121303959-T-C

23146514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121304218-T-A

23146575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121304282-T-A

23146636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121304344-C-T

http://identifiers.org/hco/16/GRCh38#23147542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121305199-C-A

23147542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121305199-C-T

23148148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121305452-G-C

23148547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121305798-G-A

http://identifiers.org/hco/16/GRCh38#23148599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121305841-C-A

23148599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121305841-C-T

http://identifiers.org/hco/16/GRCh38#23148629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#121305850-C-A

23148629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121305850-C-T

http://identifiers.org/hco/16/GRCh38#23148656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121305877-C-A

23148656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121305877-C-G

23148656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121305877-C-T

23148942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121306163-G-A

23149041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121306262-T-C

23149292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121306498-T-A

23149292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121306498-T-C

23149307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121306513-G-A

23149307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121306513-G-C

23149307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121306513-G-T

http://identifiers.org/hco/16/GRCh38#23149309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#121306515-C-A

http://identifiers.org/hco/16/GRCh38#23149315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#121306521-C-A

23149315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121306521-C-G

23149315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121306521-C-T

23149422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121306633-G-A

23149422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121306633-G-C

23149422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20060
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121306633-G-T