90383742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5590455-T-A

90383750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5590447-A-T

90383842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5590378-T-A

http://identifiers.org/hco/7/GRCh38#90383926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5590296-C-A

90383926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5590296-C-T

http://identifiers.org/hco/7/GRCh38#90384073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5590163-C-A

90384129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5590116-C-T

90384179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5590092-G-C

90384280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5590016-A-G

90384329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5589972-G-C

90384467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5589832-C-T

90384470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5589829-T-C

90384495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5589804-A-G

90384779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5589551-G-A

90384779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5589551-G-T

http://identifiers.org/hco/7/GRCh38#90384865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5589467-C-A

http://identifiers.org/hco/7/GRCh38#90384915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5589426-A-C

90384987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5589354-G-A

90385074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 5589267-T-C

90385122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 5589220-G-A

http://identifiers.org/hco/7/GRCh38#90385255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5589088-C-A

90385334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5588993-G-A

90385334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5588993-G-T

90385417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5588929-A-G

90385449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5588900-T-A

90385449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5588900-T-C

http://identifiers.org/hco/7/GRCh38#90385452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5588897-A-C

90385452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5588897-A-G

90385696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5588673-G-A

90385696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5588673-G-C

90387367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5587626-A-G

http://identifiers.org/hco/7/GRCh38#90387582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5587424-C-A

90387601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5587405-T-C

90387601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5587405-T-G

http://identifiers.org/hco/7/GRCh38#90387872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5587167-C-A

90387872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5587167-C-G

90387933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5587118-C-T

90387943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5587108-A-G

90387959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5587093-T-A

90387959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5587093-T-C

http://identifiers.org/hco/7/GRCh38#90387960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5587092-A-C

90390112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569943-A-G

90390123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569932-G-T

90390234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569821-A-G

90390253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569805-T-C

http://identifiers.org/hco/7/GRCh38#90390340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5569747-C-A

90390340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569747-C-T

90390341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569746-A-G

90390485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569591-G-A

http://identifiers.org/hco/7/GRCh38#90390530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5569549-A-C

90390532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569547-G-A

http://identifiers.org/hco/7/GRCh38#90390673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5569399-C-A

90390673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569399-C-T

90390714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569358-A-G

90390714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569358-A-T

90390721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569350-A-G

90391002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569065-G-A

90391002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 5569065-G-C

http://identifiers.org/hco/7/GRCh38#90402183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5566989-C-A

90402190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron variant
orthologous variants: 5566982-A-G

90403245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron variant
orthologous variants: 5565046-A-G

http://identifiers.org/hco/7/GRCh38#90403343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5564965-C-A

http://identifiers.org/hco/7/GRCh38#90403392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5564916-C-A

http://identifiers.org/hco/7/GRCh38#90403508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5564804-C-A

90403508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5564804-C-G

90403508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5564804-C-T

90403694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5564618-G-A

90404655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5563750-G-C

90404732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5563667-A-G

90404732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5563667-A-T

90405533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5563235-T-A

90405581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5563188-G-T

90405582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5563187-T-A

90405649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5563123-T-A

90406243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5562863-C-T

90406282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5562825-T-C

90406415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5562706-G-C

http://identifiers.org/hco/7/GRCh38#90407499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5562468-A-C

90407499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5562468-A-G

90407891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5561854-C-T

90407893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5561852-T-G

90408045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5561706-C-T

90408709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5561359-G-C

http://identifiers.org/hco/7/GRCh38#90408888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5561192-C-A

90409029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5561161-T-C

90409029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5561161-T-G

90409158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5561088-A-G

90409712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560895-A-G

http://identifiers.org/hco/7/GRCh38#90410031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5560648-C-A

90410113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560566-A-G

90410148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560535-A-G

90410216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560470-G-A

90410226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560461-G-A

90410341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560342-C-T

90410513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560192-G-A

90411164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560054-C-G

90411201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5560017-G-T

90411228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5559969-A-T

http://identifiers.org/hco/7/GRCh38#90411483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5559733-C-A

90411584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5559636-A-G

90411836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5559425-C-T

90411894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5559361-G-T

90411976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5559274-G-A

90411976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5559274-G-T

90411981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5559269-G-A

http://identifiers.org/hco/7/GRCh38#90411984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5559266-C-A

90411984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5559266-C-T

90412135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5559164-T-C

http://identifiers.org/hco/7/GRCh38#90412149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5559145-C-A

90412149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5559145-C-T

http://identifiers.org/hco/7/GRCh38#90412186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5559109-C-A

90412186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5559109-C-T

90412194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5559104-G-A

90412194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5559104-G-T

90412210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5559083-T-G

90412292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5558968-T-G

90412369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5558916-G-A

90412369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5558916-G-T

http://identifiers.org/hco/7/GRCh38#90412401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5558884-C-A

90412401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5558884-C-G

90412401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5558884-C-T

90412436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5558853-A-G

90412512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5558781-G-A

90412512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5558781-G-T

90412514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5558779-A-G

90412515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5558778-A-G

http://identifiers.org/hco/7/GRCh38#90412554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5558535-C-A

http://identifiers.org/hco/7/GRCh38#90412578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5558511-C-A

90412578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5558511-C-T

90412581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5558508-C-T

90412669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5558431-T-A

90412669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5558431-T-G

90412821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5558279-A-T

90412851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5558249-G-A

90412851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5558249-G-T

90412983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5558117-C-T

90413124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5557976-C-G

http://identifiers.org/hco/7/GRCh38#90413319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5557781-C-A

90413319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5557781-C-T

90413620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557473-T-C

90413620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557473-T-G

90413692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557401-G-T

90413706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557388-A-G

90413716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557378-G-A

90413716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557378-G-T

90413769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557342-G-A

90413769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557342-G-T

http://identifiers.org/hco/7/GRCh38#90413791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5557333-C-A

90413791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557333-C-T

90413841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557280-G-A

90413841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557280-G-T

http://identifiers.org/hco/7/GRCh38#90413873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5557248-C-A

90413873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557248-C-G

90413873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557248-C-T

90413928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557190-A-G

http://identifiers.org/hco/7/GRCh38#90413989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5557145-A-C

90414001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557135-G-A

90414001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557135-G-C

90414001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5557135-G-T

90414193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556864-A-G

http://identifiers.org/hco/7/GRCh38#90414194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5556863-A-C

90414392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556743-C-T

90414400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556736-T-C

http://identifiers.org/hco/7/GRCh38#90414437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5556705-C-A

90414437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556705-C-T

http://identifiers.org/hco/7/GRCh38#90414560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5556597-C-A

90414560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556597-C-T

90414570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556589-T-A

90414741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556438-T-G

90414867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556310-T-C

90414867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5556310-T-G

http://identifiers.org/hco/7/GRCh38#90414878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5556299-A-C

90415382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5555813-C-T

http://identifiers.org/hco/7/GRCh38#90415449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5555606-C-A

90415449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5555606-C-G

90415645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5555413-A-G

90415769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5555300-A-G

90415983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5555083-T-C

90416028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5555038-A-G

90416067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5555002-G-T

90416786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5554238-T-C

90416833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5554179-G-A

90418593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5553410-T-C

http://identifiers.org/hco/7/GRCh38#90419005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5552980-A-C

http://identifiers.org/hco/7/GRCh38#90421556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5552047-C-A

90422116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5547820-T-C

90422266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5547661-T-C

90422350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5547584-G-A

90422477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5547476-G-A

90422718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5547258-G-A

90422749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5547227-C-T

90422763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5547191-C-T

90422915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5546647-G-C

90423041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5546529-G-A

90423230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5546356-A-G

90427343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5544740-C-G

90427347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5544736-C-T

http://identifiers.org/hco/7/GRCh38#90438845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5542627-C-A

90443471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5539396-T-C

90443558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5539317-A-G

90443629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5539262-G-A

90443632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5539259-C-T

90443709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5539197-C-T

90443877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5539026-C-T

90443944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5538943-A-G

90444168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5538758-A-G

90444283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5538652-T-C

90444321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5538613-G-A

90444383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5538560-A-G

http://identifiers.org/hco/7/GRCh38#90444489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5538455-A-C

90444638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5537528-A-G

90444804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5537319-G-C

90444807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5537316-A-T

90445029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5537080-T-A

90445107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5536998-A-G

90445203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5536905-A-G

90445329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5536791-T-C

90445330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5536790-C-T

90445687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5536460-A-G

90445764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5536382-A-G

http://identifiers.org/hco/7/GRCh38#90446004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5535783-C-A

90446016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5535771-T-C

90446025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5535762-G-A

90446236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5535561-C-T

90454134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5532965-T-C

90454606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5532500-C-T

90454653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5532453-T-C

90454803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5532408-G-T

90455120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5532320-C-T

90455169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5532280-C-T

90455241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5532182-A-G

90455280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5532144-G-A

90455450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5531987-C-T

90455555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5531892-C-T

90456073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5531343-A-G

90456110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5531309-A-G

90456287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5531142-T-G

90456289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5531140-T-G

90456304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5531124-G-A

90468145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5530438-C-G

90468160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5530423-G-A

90468160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5530423-G-C

90468252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5530321-C-G

90468267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5530303-T-C

90468267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5530303-T-G

90468307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5530257-A-G

90468605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5529983-A-G

90468661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5529935-T-G

90468705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5529892-A-G

90468981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5529743-T-C

http://identifiers.org/hco/7/GRCh38#90469285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5529463-C-A

90469362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5529403-G-A

90469473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5529293-G-A

90469576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5529178-C-T

90469678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5529084-G-A

http://identifiers.org/hco/7/GRCh38#90469712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5529056-C-A

90469712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5529056-C-T

90469847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5528951-A-G

90469950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5528833-T-C

90476850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525587-T-C

90476944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525500-T-G

90476958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525477-A-G

90477006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525432-T-A

90477038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525410-T-C

90477619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5524826-G-A

90477806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5524598-T-C

90477822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5524581-A-G

90477879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5524545-C-T

http://identifiers.org/hco/7/GRCh38#90478512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5524096-A-C

90478583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5524035-G-A

90478719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5523902-A-G

90478874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5523756-G-A

http://identifiers.org/hco/7/GRCh38#90479816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5515728-C-A

90480009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5515547-T-A

90480041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5515515-C-T

90480067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5515495-A-G

90480127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5515478-C-T

90480209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5515420-A-G

90480210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5515419-T-C

90480318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5515303-C-T

90480335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5515290-C-T

90480517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514973-A-G

90480556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514934-T-C

90480624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514892-C-G

90480699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514843-T-C

90480826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514713-G-T

90480979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514607-T-G

90481534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514123-C-T

90481686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5513971-T-C

90481687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5513970-T-C

90481724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5513947-T-C

90482056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5513614-C-T

http://identifiers.org/hco/7/GRCh38#90482138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5513532-A-C

90482355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5513314-G-T

90482440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5513231-G-A

90482639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5512700-A-G

http://identifiers.org/hco/7/GRCh38#90482773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5512574-C-A

90482773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5512574-C-T

90483085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5512276-A-G

90484132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5511211-T-C

90484175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5511167-T-C

90484351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5511041-T-C

http://identifiers.org/hco/7/GRCh38#90484440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5510950-A-C

90485032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5510279-T-C

90485078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5510206-G-A

90485348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509907-T-G

90485450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509803-T-A

90485558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509697-C-T

90485570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509687-C-G

90485570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509687-C-T

90485574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509683-G-A

90485674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509571-C-G

90485895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509317-C-G

90485932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509286-C-G

90486039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509184-A-T

90486099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509124-G-A

90486102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509121-G-C

90486128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509097-G-T

90486322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508937-A-G

90486405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508879-T-G

90486437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508853-A-G

http://identifiers.org/hco/7/GRCh38#90486492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5508301-C-A

90486492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508301-C-G

90486492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508301-C-T

http://identifiers.org/hco/7/GRCh38#90486493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5508300-C-A

90486493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508300-C-T

http://identifiers.org/hco/7/GRCh38#90486517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5508278-A-C

90486517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508278-A-T

90486534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508261-T-C

90486591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508211-G-A

90486689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508114-G-A

90486940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5507860-G-T

http://identifiers.org/hco/7/GRCh38#90487264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5507438-A-C

90487264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5507438-A-G

90487290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5507412-T-G

90487298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5507404-C-G

90487949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506835-T-C

90488245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506543-C-T

90488262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506530-A-G

90488337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506452-A-G

90488501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506311-T-A

90488508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506304-T-C

90488517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506295-G-A

90489073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5505271-A-G

90489122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5505223-A-T

90489240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5505114-A-G

90489261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5505093-G-T

90489458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5504895-G-T

http://identifiers.org/hco/7/GRCh38#90489527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5504702-C-A

90489618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5504610-T-C

90489684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5504550-A-G

90489723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5504525-G-A

90490002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5504066-T-C

90490163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5503755-G-T

90490528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5503095-G-T

90490547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5503086-T-C

90490558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5503075-G-C

http://identifiers.org/hco/7/GRCh38#90490647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5503004-C-A

90490797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5502874-G-A

90490797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5502874-G-C

90491046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5502651-G-T

90491643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5502333-T-A

90492336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5501980-A-G

90492344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5501972-G-T

90492718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5501769-A-T

90492814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5501681-G-A

90493903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5501542-A-G

90494053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5501415-A-G

90494231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5501247-C-T

90494289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5501175-T-A

90494329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5500528-A-G

http://identifiers.org/hco/7/GRCh38#90494391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5500466-A-C

90494400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5500455-C-G

90494400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5500455-C-T

90494415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5500443-G-T

90494453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5500404-G-A

90494464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5500393-G-T

90494488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5500375-A-G

90499272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

90506326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5494164-T-C

90506449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5494053-C-G

90507030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5493772-T-C

90507127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5493767-T-C

90507407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5493677-A-T

90507775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5493357-C-T

http://identifiers.org/hco/7/GRCh38#90509534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5492890-A-C

90509885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5492554-G-A

90510032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5492406-T-A

http://identifiers.org/hco/7/GRCh38#90510114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5492329-C-A

90510141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5492304-T-C

90510176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5492268-A-G

90510185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5492253-A-G

90510209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5492229-G-A

90510724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491667-A-G

90510724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491667-A-T

90510809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491583-T-C

90510818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491574-C-T

90510875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491515-G-A

90510910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491481-A-G

90510915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491476-T-C

90510974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490979-C-T

90510976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490976-G-A

90511101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490871-C-T

90511107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490865-G-A

90511107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490865-G-T

90511147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490826-C-T

90511210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490764-A-G

90511260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490713-G-A

http://identifiers.org/hco/7/GRCh38#90511717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5490343-A-C

90511835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490237-T-C

http://identifiers.org/hco/7/GRCh38#90511904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5490185-C-A

90511972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490162-T-A

90511972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490162-T-C

90511985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490149-A-T

http://identifiers.org/hco/7/GRCh38#90511997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5490137-A-C

http://identifiers.org/hco/7/GRCh38#90512262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5489128-C-A

90512571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5488750-G-A

90512571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5488750-G-T

90512688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5488605-A-G

90513101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5488060-T-A

90513134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5488024-G-C

90513144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5488014-G-T

90513232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5487963-G-A

90513232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5487963-G-T

http://identifiers.org/hco/7/GRCh38#90513248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5487945-C-A

http://identifiers.org/hco/7/GRCh38#90513309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5487884-C-A

90513334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5487859-A-G