176365554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 54722898-G-A

176365554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 54722898-G-C

176365554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 54722898-G-T

http://identifiers.org/hco/5/GRCh38#176365662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54723006-C-A

176365662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: synonymous variant
orthologous variants: 54723006-C-T

176365778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54723113-G-A

176365778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54723113-G-C

176365899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54723189-G-A

176365949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54723220-G-A

176365949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54723220-G-T

176366472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: synonymous_variant, undefined
orthologous variants: 54723652-G-A

176366472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: synonymous_variant, undefined
orthologous variants: 54723652-G-C

176366587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54723770-C-G

176366587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54723770-C-T

http://identifiers.org/hco/5/GRCh38#176366658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54723836-C-A

176366770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54723941-C-T

176366901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54724058-C-T

176366928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54724085-T-C

176367651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725672-C-G

176367747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725764-T-C

http://identifiers.org/hco/5/GRCh38#176367804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54725817-C-A

176367804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725817-C-T

176367853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725871-A-T

http://identifiers.org/hco/5/GRCh38#176367907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54725928-C-A

176367907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725928-C-T

176367963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54725968-G-A

176368003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54726008-G-C

176368459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726380-G-A

176368695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726529-C-T

176368696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726530-G-A

176368736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726568-G-A

176368832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54726631-C-T

176369060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54726843-T-G

176369070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54726850-G-C

176369083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 54726860-G-A

176369083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54726860-G-T

176369377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54727081-T-C

176369381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54727085-T-A

176371730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant
orthologous variants: 54728542-C-G

176371730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 54728542-C-T

http://identifiers.org/hco/5/GRCh38#176371952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54728767-C-A

176371952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728767-C-T

176371953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728768-T-C

http://identifiers.org/hco/5/GRCh38#176371970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54728785-C-A

176371970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728785-C-T

176372006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54728821-C-T

176372031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728834-G-T

176372049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728840-A-T

176372053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728844-A-G

176372058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728849-G-A

http://identifiers.org/hco/5/GRCh38#176372062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54728853-C-A

http://identifiers.org/hco/5/GRCh38#176372195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54728944-C-A

176372195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728944-C-G

176372195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728944-C-T

176372207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728966-A-G

http://identifiers.org/hco/5/GRCh38#176372210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54728969-C-A

176372210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54728969-C-T

176372278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729033-T-C

176372278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729033-T-G

http://identifiers.org/hco/5/GRCh38#176372389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54729156-C-A

176372389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729156-C-T

http://identifiers.org/hco/5/GRCh38#176372418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54729177-C-A

176372418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54729177-C-T

176372522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729272-G-A

176372522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729272-G-T

http://identifiers.org/hco/5/GRCh38#176372590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54729335-C-A

176372590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729335-C-T

176372740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729469-T-C

http://identifiers.org/hco/5/GRCh38#176372769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54729492-C-A

176372769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729492-C-G

http://identifiers.org/hco/5/GRCh38#176372858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54729605-C-A

176372858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729605-C-T

176373029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729787-A-G

176373029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729787-A-T

176373031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729789-C-T

176373173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729810-C-T

176373186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729820-C-T

http://identifiers.org/hco/5/GRCh38#176373325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54729950-C-A

176373325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729950-C-G

176373325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729950-C-T

176373348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54729973-T-G

176373516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54730139-T-C

176373525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54730146-T-C

http://identifiers.org/hco/5/GRCh38#176373607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54730224-C-A

176383378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732131-G-A

176383378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732131-G-T

176383400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732153-A-G

176383469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732224-T-G

176383490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732245-T-C

176383504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732258-A-T

176383518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732272-G-C

http://identifiers.org/hco/5/GRCh38#176383633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54732361-A-C

176383712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732433-C-T

http://identifiers.org/hco/5/GRCh38#176383794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54732513-C-A

176383794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732513-C-T

176383815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732528-G-A

176383815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732528-G-T

176383829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732543-G-T

http://identifiers.org/hco/5/GRCh38#176383891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54732596-C-A

176383891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54732596-C-T

176383978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54732685-T-C

176384052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54732765-C-T

176384079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54732789-G-A

176384079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54732789-G-T

176384091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54732801-C-G

176384091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54732801-C-T

176384282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 54733145-C-T

176384306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 54733169-G-A

176384456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733324-T-A

176384477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733345-C-T

176384486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733354-G-C

176384486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733354-G-T

176385182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 54733587-G-A

176385182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 54733587-G-T

176385227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54733639-G-T

176385235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54733647-C-G

176385235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54733647-C-T

176385350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733759-G-A

176385352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733761-G-A

176385352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733761-G-C

176385352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733761-G-T

176385372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733779-T-G

http://identifiers.org/hco/5/GRCh38#176385398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54733805-C-A

176385398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733805-C-T

176385582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733946-G-A

176385582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733946-G-T

176385623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54733990-T-G

176385777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54734131-C-T

http://identifiers.org/hco/5/GRCh38#176385822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54734159-C-A

http://identifiers.org/hco/5/GRCh38#176385823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54734160-A-C

176385825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54734162-G-A

176385827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54734164-G-T

176385864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54734200-T-C

176385986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54734881-T-G

176386447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54736059-A-T

176386531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54736122-T-C

176386694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54736275-G-A

176386829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54736400-A-G

176386878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54736449-C-G

176386878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 54736449-C-T

http://identifiers.org/hco/5/GRCh38#176386995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54736577-C-A

176386995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54736577-C-T

http://identifiers.org/hco/5/GRCh38#176387811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54737053-A-C

176387850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737112-G-A

176387907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737163-G-A

176387979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737212-T-G

176388111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737316-G-T

http://identifiers.org/hco/5/GRCh38#176388125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54737343-C-A

176388125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737343-C-T

http://identifiers.org/hco/5/GRCh38#176388127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54737345-C-A

176388127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737345-C-T

176388129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737347-G-C

176388129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737347-G-T

176388156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737374-T-C

176388156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737374-T-G

http://identifiers.org/hco/5/GRCh38#176388158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54737376-C-A

176388158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737376-C-T

176388196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737420-G-A

176388197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737421-T-A

176388197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737421-T-C

176388197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737421-T-G

176388219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737460-C-T

http://identifiers.org/hco/5/GRCh38#176388224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54737465-C-A

176388239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54737480-C-T

176388299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54737540-T-C

176388303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 54737544-G-A

176388303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant, undefined
orthologous variants: 54737544-G-T

176388305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54737546-A-G

176388334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 54737575-G-A

176388378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54737625-C-G

176388378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 54737625-C-T

176388438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 54737679-G-A

176388438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant, undefined
orthologous variants: 54737679-G-T

176388540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54737781-C-T

http://identifiers.org/hco/5/GRCh38#176388603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54737866-A-C

176388700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54737956-G-A

176388718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54737974-T-C

http://identifiers.org/hco/5/GRCh38#176388729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54737985-C-A

176388752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54738007-C-T

http://identifiers.org/hco/5/GRCh38#176388762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54738016-C-A

176388803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54738061-G-A

176388803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54738061-G-T

176388809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54738067-G-A

176388966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 54738225-A-G

176388966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 54738225-A-T

176388995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738254-T-G

176388996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738255-G-A

http://identifiers.org/hco/5/GRCh38#176389019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54738278-C-A

176389020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738279-G-A

176389020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738279-G-T

176389035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738295-G-A

176389054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738311-G-T

http://identifiers.org/hco/5/GRCh38#176389055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54738312-C-A

176389067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738327-G-A

176389069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738329-A-G

176389161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738412-C-T

176389174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738423-G-A

http://identifiers.org/hco/5/GRCh38#176389179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54738428-C-A

176389179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738428-C-G

176389259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738461-G-A

176389259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, undefined
orthologous variants: 54738461-G-C

176389502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54738708-A-G

176389521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54738724-T-G

http://identifiers.org/hco/5/GRCh38#176389566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54738765-C-A

http://identifiers.org/hco/5/GRCh38#176389627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54738827-C-A

176389636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54738836-A-G

176389677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54738889-G-T

176389845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739094-T-C

176389855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739101-A-G

176389858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739104-T-G

176389891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739160-G-A

176389891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739160-G-T

176389901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739170-G-A

176389901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739170-G-T

176390012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739309-A-G

176391011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739830-C-T

176391012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739831-G-A

176391012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739831-G-C

176391183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54739990-T-C

176391755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54740640-A-G

176391817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54740700-C-T

http://identifiers.org/hco/5/GRCh38#176391954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54740840-A-C

176392113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54741007-G-A

176392145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54741044-T-G

176392219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54741112-C-G

176392352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron variant
orthologous variants: 54741254-T-C

http://identifiers.org/hco/5/GRCh38#176392682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54741591-C-A

176392682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54741591-C-T

176393046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54741954-C-T

176393097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54742007-G-T

176393134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54742054-C-T

176393187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54742198-T-G

176393798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54742820-T-G

176394256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54743402-A-G

176394320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54743431-C-G

176394882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54743549-T-C

176395363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54743948-C-T

176395490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54744095-G-A

176395775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54744417-A-G

176395793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54744425-C-T

http://identifiers.org/hco/5/GRCh38#176396333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54744687-C-A

http://identifiers.org/hco/5/GRCh38#176396338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54744692-A-C

http://identifiers.org/hco/5/GRCh38#176396385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54744747-C-A

176396423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54744786-T-C

176396428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54744793-T-C

176396430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54744795-G-A

176396430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54744795-G-T

176397224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54745614-C-T

176397258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54745648-G-A

176397412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746357-T-C

176397456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746402-T-A

176397456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746402-T-G

http://identifiers.org/hco/5/GRCh38#176397486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54746436-C-A

176397578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746523-G-A

176397578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746523-G-C

176397578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746523-G-T

176397682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54746610-T-C

176397774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746702-G-A

176397774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746702-G-T

http://identifiers.org/hco/5/GRCh38#176397809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54746743-C-A

176397809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746743-C-T

176397847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746767-G-A

176397847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746767-G-C

176397847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54746767-G-T

176397922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 54746849-G-A

176397922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 54746849-G-T

176398078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747001-G-A

176398082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747005-G-A

176398082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747005-G-C

176398084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747007-A-G

176398134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747062-G-A

176398134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747062-G-T

176398144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747085-G-T

http://identifiers.org/hco/5/GRCh38#176398159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54747101-A-C

176398171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747111-T-C

http://identifiers.org/hco/5/GRCh38#176398194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54747135-C-A

176398194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747135-C-T

176398225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747163-G-A

176398348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54747241-C-T

176402710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54750065-G-A