http://identifiers.org/hco/9/GRCh38#35814477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43655963-C-A

35814477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43655963-C-T

http://identifiers.org/hco/9/GRCh38#35814481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43655969-A-C

35814481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43655969-A-G

35814517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656000-G-A

35814517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656000-G-T

35814529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656012-T-C

35814529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656012-T-G

http://identifiers.org/hco/9/GRCh38#35814598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43656081-C-A

35814598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656081-C-T

35814636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656108-A-G

http://identifiers.org/hco/9/GRCh38#35814645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43656117-A-C

35814645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656117-A-G

35814645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656117-A-T

35814650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656122-A-G

35814669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656143-G-A

35814705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656180-G-A

35814705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656180-G-C

35814705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656180-G-T

http://identifiers.org/hco/9/GRCh38#35814757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43656238-C-A

35814757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656238-C-T

35814768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656249-A-G

http://identifiers.org/hco/9/GRCh38#35814800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43656284-C-A

35814800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656284-C-T

http://identifiers.org/hco/9/GRCh38#35814912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43656372-A-C

http://identifiers.org/hco/9/GRCh38#35814916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43656376-C-A

35814916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656376-C-G

35814916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656376-C-T

http://identifiers.org/hco/9/GRCh38#35814923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43656383-C-A

35814923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 43656383-C-T

35814942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656402-G-A

35814942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656402-G-C

35814942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43656402-G-T

35814957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656417-G-A

35814957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656417-G-C

35814957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43656417-G-T

35815342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43656660-T-A

35815342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43656660-T-G

http://identifiers.org/hco/9/GRCh38#35815357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43656675-A-C

35815357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43656675-A-G

35815357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43656675-A-T

35815414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43656705-T-C

35815430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43656721-T-C

35815430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43656721-T-G

35815514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, undefined
orthologous variants: 43656814-C-G

35816429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43657832-T-C

35816534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43657917-T-G

35816540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43657923-A-G

35816614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43657988-T-G

35816671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658025-G-A

35816771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658114-G-C

35816873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658211-T-C

35817189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658457-T-C

35817190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658458-G-A

35817206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658472-T-A

35817206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658472-T-C

http://identifiers.org/hco/9/GRCh38#35817211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43658478-C-A

http://identifiers.org/hco/9/GRCh38#35817267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43658538-C-A

http://identifiers.org/hco/9/GRCh38#35817276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43658547-C-A

35817276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658547-C-T

http://identifiers.org/hco/9/GRCh38#35817283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43658558-C-A

35817283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658558-C-G

35817283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658558-C-T

35817284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658559-T-C

35817292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658567-G-C

35817301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658591-T-C

35817302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658592-G-A

35817304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658594-A-G

35817338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658634-T-C

35817358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658653-T-A

35817474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658766-T-A

35817517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658805-C-T

35817595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658880-C-T

http://identifiers.org/hco/9/GRCh38#35817600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43658885-C-A

35817670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43658954-T-C

35817905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659125-T-A

35817905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659125-T-C

35817920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659140-T-C

http://identifiers.org/hco/9/GRCh38#35817930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659148-C-A

35817930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659148-C-T

http://identifiers.org/hco/9/GRCh38#35817972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659189-C-A

http://identifiers.org/hco/9/GRCh38#35817985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659202-C-A

35817985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659202-C-G

http://identifiers.org/hco/9/GRCh38#35818013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659226-C-A

35818044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659257-G-T

http://identifiers.org/hco/9/GRCh38#35818047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659260-C-A

http://identifiers.org/hco/9/GRCh38#35818076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659288-C-A

35818076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659288-C-T

35818120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659331-G-A

35818120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659331-G-T

http://identifiers.org/hco/9/GRCh38#35818131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659340-C-A

35818131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659340-C-T

http://identifiers.org/hco/9/GRCh38#35818183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659373-C-A

35818196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659385-A-G

35818196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659385-A-T

35818311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659497-G-A

35818346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659532-G-A

35818346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659532-G-C

35818346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659532-G-T

35818355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659535-A-G

35818355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659535-A-T

http://identifiers.org/hco/9/GRCh38#35818361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659541-C-A

35818393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659579-G-T

http://identifiers.org/hco/9/GRCh38#35818405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659591-C-A

35818405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659591-C-G

35818405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659591-C-T

http://identifiers.org/hco/9/GRCh38#35818475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659661-A-C

35818475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43659661-A-G

35818490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43659676-G-T

35818520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659706-G-A

35818520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659706-G-T

http://identifiers.org/hco/9/GRCh38#35818751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659911-C-A

35818751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659911-C-T

35818768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659923-G-T

http://identifiers.org/hco/9/GRCh38#35818789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43659940-C-A

35818789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659940-C-T

35818790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659941-G-A

35818790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659941-G-T

35818804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659955-G-T

35818883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 43660030-G-T

35818942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43660089-G-A

35818942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43660089-G-T

http://identifiers.org/hco/9/GRCh38#35819082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43660209-C-A

35819082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660209-C-G

35819085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660212-C-G

35819085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660212-C-T

http://identifiers.org/hco/9/GRCh38#35819157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43660243-C-A

35819157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660243-C-T

http://identifiers.org/hco/9/GRCh38#35819204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43660289-C-A

35819204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43660289-C-T

http://identifiers.org/hco/9/GRCh38#35819267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43660352-C-A

35819267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43660352-C-T

35819284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43660369-C-T

35819417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660500-T-C

35819847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660600-T-A

35819847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660600-T-G

http://identifiers.org/hco/9/GRCh38#35819942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43660696-A-C

35819942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43660696-A-G

35819975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43660729-G-C

http://identifiers.org/hco/9/GRCh38#35820066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43660830-A-C

35820066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660830-A-G

35820100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660857-T-C

35820100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660857-T-G

35820104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660861-T-A

35820104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660861-T-C

35820152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660888-T-G

35820281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661010-G-A

35820321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661044-T-C

35820531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661238-G-C

35820531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661238-G-T

35820695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661400-G-A

35821038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661719-T-G

35821040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661721-T-C

35821443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43661915-G-C

35821445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43661917-C-G

35821467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 43661939-T-A

35821635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 43662095-T-C

35821685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662150-G-T

http://identifiers.org/hco/9/GRCh38#35821688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43662153-C-A

35821688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662153-C-G

35821688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662153-C-T

35821772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662227-A-G

35821802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662257-G-A

35821806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662261-C-T

35821844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662322-G-A

35822036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662465-C-T

35822067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662496-A-G

35822067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662496-A-T

35822106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662533-A-G

35822309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662686-G-A

35822851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662855-A-G

35822971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662955-G-A

35823215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663324-T-C

35823224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663333-G-T

35823392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663558-T-C

35823612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663747-G-A

35823820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664202-A-G

http://identifiers.org/hco/9/GRCh38#35823851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43664243-A-C

http://identifiers.org/hco/9/GRCh38#35823962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43664384-C-A

35824132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664569-G-C

35824205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664635-A-G

35824324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664747-T-C

35824971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43665220-G-A

35825477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43665705-G-T

35825525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43665748-T-A

35825797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43666059-T-C

35825807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43666069-A-G

35825823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43666113-T-A

35825840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43666144-G-A

35825843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43666147-T-C

35825843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43666147-T-G

35825897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43666243-T-C

35825898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 43666244-A-G

35826325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43666772-T-G

35826491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43666941-G-C

35826641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43667050-G-A

35826793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 43667135-T-C

http://identifiers.org/hco/9/GRCh38#35826839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43667162-C-A

35826839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43667162-C-T

35826843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43667166-G-A

35826843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43667166-G-T

35826893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43667188-G-A

http://identifiers.org/hco/9/GRCh38#35826961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43667244-C-A

35827111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43667324-C-T

35827250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43667441-A-G

35827363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43667558-T-G

http://identifiers.org/hco/9/GRCh38#35828410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43668523-A-C

35828410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43668523-A-G

35828484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43668614-G-A

35828516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43668646-G-A

35828516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43668646-G-T

35828821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43668928-G-C

35828821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43668928-G-T

http://identifiers.org/hco/9/GRCh38#35828829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43668936-C-A

35828829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43668936-C-G

http://identifiers.org/hco/9/GRCh38#35829096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43669170-C-A

35829096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, undefined
orthologous variants: 43669170-C-T

35829253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43669297-G-A

35829253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43669297-G-T

35829266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43669307-G-C

35829266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43669307-G-T

http://identifiers.org/hco/9/GRCh38#35829312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43669353-C-A

35829312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43669353-C-T

http://identifiers.org/hco/9/GRCh38#35829402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43669460-C-A

35829402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43669460-C-G

35829402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43669460-C-T

http://identifiers.org/hco/9/GRCh38#35829517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43669575-C-A

35829517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43669575-C-G

35829517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43669575-C-T

http://identifiers.org/hco/9/GRCh38#35829699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43669775-C-A

35829699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43669775-C-T

http://identifiers.org/hco/9/GRCh38#35829727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43669803-C-A

35829727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43669803-C-T

http://identifiers.org/hco/9/GRCh38#35829807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43669886-C-A

35829807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43669886-C-G

35829807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43669886-C-T

35829816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43669895-G-A

35829816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43669895-G-C

35829816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43669895-G-T

http://identifiers.org/hco/9/GRCh38#35829963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43670042-C-A

35829963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43670042-C-T

35830011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670086-T-G

35830073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670159-A-G

35830659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670737-T-G

35831127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671121-C-T

35832245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671932-G-A

35832716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672247-T-C

35832899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672419-G-T

35833045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672555-C-T

35833244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672755-G-T

35833297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672792-C-T

35833314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672811-C-T

http://identifiers.org/hco/9/GRCh38#35833737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43673243-C-A

35833737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673243-C-G

35833849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673351-C-T

35834285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43673766-A-G

35834314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43673795-C-T

http://identifiers.org/hco/9/GRCh38#35834334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43673798-C-A

35834335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43673799-A-G

35834336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43673800-G-A

35834336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43673800-G-T

http://identifiers.org/hco/9/GRCh38#35834453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43673892-C-A

35834453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43673892-C-T

35834480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43673919-T-C

35834558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43673997-T-A

35834558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43673997-T-C

http://identifiers.org/hco/9/GRCh38#35834782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43674229-C-A

35834782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43674229-C-T

35834869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674313-G-A

35835206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43674632-C-T

http://identifiers.org/hco/9/GRCh38#35835250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43674668-A-C

35835250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43674668-A-G

35835288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43674704-G-A

35835288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43674704-G-T

35835337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43674752-G-A

35835337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43674752-G-C

http://identifiers.org/hco/9/GRCh38#35835350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43674765-C-A

35835350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43674765-C-T

35835404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43674809-G-C

35835404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43674809-G-T

http://identifiers.org/hco/9/GRCh38#35835438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43674830-C-A

35835612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674997-A-G

http://identifiers.org/hco/9/GRCh38#35835641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43675026-C-A

35835641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675026-C-T

35836058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675381-A-T

http://identifiers.org/hco/9/GRCh38#35836080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43675403-A-C

35836126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675445-G-A

35836263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675523-A-G

35836340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675590-T-C

35836360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675613-G-T

35836361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675614-G-A

35836798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675985-C-G

35837074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43676198-G-A

35838040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677058-T-G

35838053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677071-G-A

35838086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677091-G-A

35838122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677144-C-T

35838265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677284-A-T

http://identifiers.org/hco/9/GRCh38#35838620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43677630-A-C

35838846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677825-G-C

35838897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677857-A-G

35839325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678465-C-T

http://identifiers.org/hco/9/GRCh38#35839575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43678766-C-A

35839614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678794-G-T

35839832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678983-C-G

35839949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43679156-G-A

35839961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43679168-C-T

35840036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43679242-G-A

35840366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43679590-C-T

35841027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680552-G-A

35841027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680552-G-C

35841027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680552-G-T

35841184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43680709-G-A

35841184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43680709-G-C

35841184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43680709-G-T

http://identifiers.org/hco/9/GRCh38#35841274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43680799-C-A

http://identifiers.org/hco/9/GRCh38#35841302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43680813-C-A

35841302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680813-C-T

http://identifiers.org/hco/9/GRCh38#35841314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43680821-C-A

http://identifiers.org/hco/9/GRCh38#35841327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43680832-C-A

35841327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680832-C-T

35841370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680878-G-T

35841374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680882-G-T

35841739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43681259-A-G

35841797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681317-C-T

35841798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681318-A-G

35841798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681318-A-T

35841834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681362-T-G

http://identifiers.org/hco/9/GRCh38#35841941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43681460-C-A

35841941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681460-C-T

35842100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681617-C-T

35842158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681671-A-G

35842231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681781-C-T

http://identifiers.org/hco/9/GRCh38#35842295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43681859-A-C

35842295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681859-A-T

35842317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681882-G-A

35842317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681882-G-T

http://identifiers.org/hco/9/GRCh38#35842318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43681883-C-A

35842318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681883-C-G

35842361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681928-G-A

35842361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681928-G-T

35842477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43682044-C-T

http://identifiers.org/hco/9/GRCh38#35842485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43682052-C-A

35842485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43682052-C-T

35842505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43682072-G-A

35842505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43682072-G-T

35842528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43682095-C-G

35842528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43682095-C-T

35842609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43682176-T-C

35842708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43682275-G-T

http://identifiers.org/hco/9/GRCh38#35842716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43682283-C-A

35842716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43682283-C-T

35842758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682320-G-T

35842762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682324-G-A

35842762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682324-G-T

35842767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682329-G-T

http://identifiers.org/hco/9/GRCh38#35842835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43682397-C-A

35842835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682397-C-T

35842968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682504-C-T

35845037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684143-C-T

35845097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684200-A-G

35845255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684444-G-A

35845255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684444-G-T

http://identifiers.org/hco/9/GRCh38#35845300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43684496-C-A

35845354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684564-G-A

35845367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684577-C-T

35845474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684689-G-C

35845555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684834-A-G

35845730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43685050-G-A

35845730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43685050-G-T

http://identifiers.org/hco/9/GRCh38#35845878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43685180-C-A

35845878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43685180-C-T

35845966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43685288-C-G

35845966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43685288-C-T

35846254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43685522-T-G

35846493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 43685752-G-A

35846493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 43685752-G-T

http://identifiers.org/hco/9/GRCh38#35846589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: missense_variant, stop_gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#43685848-C-A

35846589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 43685848-C-T

http://identifiers.org/hco/9/GRCh38#35846595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43685854-C-A

35846620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43685879-G-A

35846620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43685879-G-C

35846620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43685879-G-T

35846639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43685889-G-T

35846783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43685977-G-T

35846802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43685996-C-T

35846827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: synonymous variant
orthologous variants: 43686021-C-T

35847039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, stop_gained
orthologous variants: 43686232-G-A

35847263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43686421-G-A

35847263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43686421-G-T

35847665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43686956-G-A

35852265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43688667-A-G

35852265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43688667-A-T

35852392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43688797-G-T

35852603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43688975-G-A

35852603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43688975-G-C

35852603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43688975-G-T

35852663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43689034-T-C

35852665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43689052-C-G

35852683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43689286-A-G

35852811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43689411-T-C

35852940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 43689540-T-C

http://identifiers.org/hco/9/GRCh38#35852981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43689581-C-A

35853170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: synonymous variant
orthologous variants: 43689720-G-C

http://identifiers.org/hco/9/GRCh38#35853349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43689901-C-A

35853349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43689901-C-T

http://identifiers.org/hco/9/GRCh38#35853387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43689939-A-C

35853483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron variant
orthologous variants: 43690005-C-T

35853501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 43690023-C-T

http://identifiers.org/hco/9/GRCh38#35853719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43690241-A-C

35853719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant
orthologous variants: 43690241-A-G

35853729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 43690251-A-G

http://identifiers.org/hco/9/GRCh38#35853774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43690296-C-A

35853774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 43690296-C-T

http://identifiers.org/hco/9/GRCh38#35853792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43690314-C-A

35853792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 43690314-C-G

http://identifiers.org/hco/9/GRCh38#35854038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43690558-A-C

35854042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690562-T-C

35854097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690615-G-A

http://identifiers.org/hco/9/GRCh38#35854121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43690637-C-A

http://identifiers.org/hco/9/GRCh38#35854152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43690669-A-C

35854152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690669-A-G

35854152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690669-A-T

35854156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690673-A-G

35854171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690688-G-A

35854240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690743-C-T

35854255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690758-G-T

35854319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690798-G-T

35854332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690811-A-G

35854393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43690870-G-T

35854510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691007-G-A

35854510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691007-G-T

http://identifiers.org/hco/9/GRCh38#35854525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43691022-C-A

35854586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691081-T-C

35854739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691228-C-T

35854878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691583-T-C

35855000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691741-G-A

35855000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691741-G-C

35855000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691741-G-T

35855193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691918-G-A

35855193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691918-G-T

35855261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691973-G-T

35855279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43691990-C-T

35855299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43692015-T-C

http://identifiers.org/hco/9/GRCh38#35855313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43692029-C-A

35855461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43692184-T-C

35855891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43692721-T-G

35855941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43692795-G-A

35855942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43692796-T-C

http://identifiers.org/hco/9/GRCh38#35856234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43693064-A-C

35856272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693088-A-G

35856290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693106-T-C

35856424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693186-T-G

http://identifiers.org/hco/9/GRCh38#35856507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43693284-C-A

35856715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693470-T-A

35856780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693527-G-T

http://identifiers.org/hco/9/GRCh38#35856805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43693561-C-A

35856805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693561-C-T

35856884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693642-A-G

35856894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693668-G-A

http://identifiers.org/hco/9/GRCh38#35857121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43693804-C-A

35857121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693804-C-G

35857185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693867-G-C

35857185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43693867-G-T

35857499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43694117-A-T

35857563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43694176-G-T

35858394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43695604-T-C

35858436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43695646-C-T

http://identifiers.org/hco/9/GRCh38#35858567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43695790-C-A

35858586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43695798-G-A

35858649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43695856-G-A

35858649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43695856-G-C

35858649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43695856-G-T

35858728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43695918-G-A

http://identifiers.org/hco/9/GRCh38#35858834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43696025-C-A

http://identifiers.org/hco/9/GRCh38#35858898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43696077-C-A

35858898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43696077-C-T

35858904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43696083-A-G

35858919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43696098-C-T

35858932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43696114-G-A

35858932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43696114-G-T

35859027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43696207-G-A

35859027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43696207-G-T

35859124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696305-G-A

35859124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696305-G-C

35859124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696305-G-T

35859136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696317-G-A

35859136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696317-G-T

http://identifiers.org/hco/9/GRCh38#35859153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43696334-C-A

35859153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696334-C-T

35859253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696434-T-A

35859253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696434-T-C

http://identifiers.org/hco/9/GRCh38#35859290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43696471-C-A

35859290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696471-C-G

35859290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696471-C-T

35859361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696542-G-T

35859379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696560-G-A

35859380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696561-G-A

35859380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696561-G-T

35859392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696573-A-G

35859490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696677-G-A

35859491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696678-T-C

35859579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696766-T-C

http://identifiers.org/hco/9/GRCh38#35859593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43696780-C-A

35859593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696780-C-G

35859593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696780-C-T

35859604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696791-G-A

35859604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696791-G-C

35859604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696791-G-T

http://identifiers.org/hco/9/GRCh38#35859634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43696821-C-A

35859634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696821-C-T

35859721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43696908-G-T

35859810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43697001-G-T

http://identifiers.org/hco/9/GRCh38#35859840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43697031-C-A

35859840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43697031-C-T

http://identifiers.org/hco/9/GRCh38#35859912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43697103-C-A

35859945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43697136-G-A

35859945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43697136-G-T

35860121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697296-G-T

35860134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697307-T-C

35860309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697483-G-T

35860352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697516-G-T

35860465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697629-G-T

35860512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697661-T-C

35862226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697962-G-A

35862226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697962-G-T

http://identifiers.org/hco/9/GRCh38#35862238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43697974-C-A

35862238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43697974-C-T

35862278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698016-T-C

35862330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698047-A-G

35862360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698072-G-C

35862360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698072-G-T

35862362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698074-G-A

http://identifiers.org/hco/9/GRCh38#35862503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43698169-C-A

35862527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698192-T-C

35862528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698193-G-C

35862528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698193-G-T

35862548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698204-G-A

35862548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698204-G-C

35862579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698224-A-G

http://identifiers.org/hco/9/GRCh38#35862706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43698346-C-A

http://identifiers.org/hco/9/GRCh38#35862797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43698424-C-A

35862797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698424-C-T

35862909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698585-T-C

http://identifiers.org/hco/9/GRCh38#35862916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43698592-C-A

35862940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698615-T-C

http://identifiers.org/hco/9/GRCh38#35863120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43698679-C-A

35863120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698679-C-T

35863325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698800-A-G

35863354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698828-T-C

35863496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698944-G-A

35863544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698968-G-A

35863544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43698968-G-T

35863648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699071-C-T

35863783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699214-G-A

35863783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699214-G-T

http://identifiers.org/hco/9/GRCh38#35863810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43699241-C-A

35863874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699305-G-A

35863874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699305-G-T

35863892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699323-T-C

35864091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699639-A-G

35864110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699660-T-C

35864125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699675-G-T

35864365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699922-G-T

35864436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43699991-G-C

35864599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700577-A-G

35864699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700674-A-G

35864788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700758-G-A

35864791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700761-T-C

35864823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700793-G-A

35864823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700793-G-T

35864832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700802-G-T

35864835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700805-T-C

35864847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700829-G-A

35864847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43700829-G-T

35865055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43701012-T-C

35865136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43701077-C-G

35865137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43701078-A-G

35865176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43701116-T-C

http://identifiers.org/hco/9/GRCh38#35865184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43701124-C-A

35865195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43701135-G-A

35865195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43701135-G-T

35865462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21427
most severe consequence: 3 prime UTR variant
orthologous variants: 43701419-T-C