44975348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122941580-C-T

44975481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122941655-G-T

44975635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122941834-G-A

44975674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122941878-A-G

http://identifiers.org/hco/3/GRCh38#44975910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122942038-C-A

44976021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122942110-G-A

44976021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122942110-G-T

44976103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122942190-G-A

44976103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122942190-G-T

http://identifiers.org/hco/3/GRCh38#44976170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122942255-A-C

44976170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122942255-A-G

44976170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122942255-A-T

http://identifiers.org/hco/3/GRCh38#44976366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122942404-C-A

44976366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122942404-C-G

44976366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122942404-C-T

44976391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122942421-G-A

44976391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122942421-G-T

44976460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122942455-A-G

44976509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122942493-T-G

44976636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122942619-G-A

44976777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122942751-G-A

44976850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122942864-G-C

44977376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122943394-C-G

44977464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122943483-T-G

44982038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944095-T-C

44982098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944159-G-C

44982388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944533-T-C

44982438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944564-G-T

44982772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944850-T-C

44982859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944928-G-A

44982859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944928-G-C

44982859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944928-G-T

44982896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122944966-C-T

http://identifiers.org/hco/3/GRCh38#44983087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122945128-A-C

44987270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122946510-A-G

44987751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122946767-T-C

44988588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122947482-G-A

44988783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122947658-C-T

44988784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122947659-A-G

44988823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122947693-A-G

44988847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122947721-A-G

44988914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122947788-A-G

44989232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122948048-G-A

http://identifiers.org/hco/3/GRCh38#44989403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122948207-C-A

44989405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122948209-G-A

44989405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122948209-G-T

44989433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122948234-A-T

44990296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122949056-G-A

44990524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122949913-A-G

http://identifiers.org/hco/3/GRCh38#44990548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122949924-C-A

44990555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122949931-A-G

44990559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122949935-C-G

44990559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122949935-C-T

http://identifiers.org/hco/3/GRCh38#44990566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122949942-A-C

44990636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122950021-A-G

44990688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122950062-C-T

44990800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122950159-G-C

44991220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122950455-A-G

44991225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

44991252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122950479-A-G

44991519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122950698-A-G

http://identifiers.org/hco/3/GRCh38#44991539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122950718-A-C

44991668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122951312-A-G

44991962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952089-C-T

44992002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952125-C-T

http://identifiers.org/hco/3/GRCh38#44992253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122952314-A-C

44992316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952365-G-A

44992320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952369-A-T

44992530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952560-C-G

44992664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952701-G-A

44992759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952784-T-G

44992904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952909-T-G

44992948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122952953-A-G

44993073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122953042-T-C

44993114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122953083-G-A

44993564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122953325-G-A

http://identifiers.org/hco/3/GRCh38#44994071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122953827-A-C

44994235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122954058-T-A

44994587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122954659-G-A

44995417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122955451-C-T

44995541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122955581-A-T

44995557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122955597-A-G

44995682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122955714-G-A

44995688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122955720-A-G

44995926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122955947-C-G

44996491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122956303-G-T

44996569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122956387-T-A

http://identifiers.org/hco/3/GRCh38#44996691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122956470-C-A

44996893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122956636-A-G

44996910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122956653-T-C

44996937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122956681-G-A

44996974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122956723-G-A

http://identifiers.org/hco/3/GRCh38#44996983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122956753-C-A

44997275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122957059-G-A

44997283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122957065-T-C

44997389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122957185-G-T

44997453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122957248-C-T

44997491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122957286-C-T

45000980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122958913-A-G

45001059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122958981-A-G

http://identifiers.org/hco/3/GRCh38#45001480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122959534-C-A

45001480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122959534-C-T

45001489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122959541-A-G

45001490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122959542-T-G

http://identifiers.org/hco/3/GRCh38#45001631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122959683-C-A

45001631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122959683-C-G

45001631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122959683-C-T

45001666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122959706-A-G

45001684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122959726-T-C

http://identifiers.org/hco/3/GRCh38#45001747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122959772-A-C

http://identifiers.org/hco/3/GRCh38#45001752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122959777-A-C

45001752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122959777-A-G

45005238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122959838-G-T

45005490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122960091-T-C

45005490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122960091-T-G

45005592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122960188-T-C

45007305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122960849-G-A

45007358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122960894-A-G

45007358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122960894-A-T

45007389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122960921-C-G

45007510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122961040-G-T

45007581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961111-G-A

45007581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961111-G-C

45007581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961111-G-T

45007595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961125-G-A

http://identifiers.org/hco/3/GRCh38#45007614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122961137-C-A

45007614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961137-C-G

45007614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961137-C-T

http://identifiers.org/hco/3/GRCh38#45007675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122961193-C-A

45007675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961193-C-T

http://identifiers.org/hco/3/GRCh38#45007727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122961229-C-A

45007727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961229-C-T

45007754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122961241-G-T

45009143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122963491-C-T

45009362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122963610-C-T

45009526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122963721-A-T

45009795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122963957-C-G

45009809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122963971-G-A

45010173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122964256-T-C

45010578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122964351-T-C

45010829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122964548-A-G

45010975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122964672-G-A

45011000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122964722-G-A

45011155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122964891-G-A

45011178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122964910-T-C

45011265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122964994-G-A

45011265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122964994-G-T

45011430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122965149-A-G

45011478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122965197-G-A

http://identifiers.org/hco/3/GRCh38#45011505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122965224-C-A

45011505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122965224-C-G

45011762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122965961-C-G

45012050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122966351-A-G

45012151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122966414-A-G

45012187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122966449-A-G

45012349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122966611-G-T

http://identifiers.org/hco/3/GRCh38#45012458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122966717-C-A

45012585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122966831-G-T

45012624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122966865-G-T

45012629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122966870-A-G

45012657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122966897-A-G

45012674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122966914-G-T

45016931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122967358-T-C

45017076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122967454-G-A

45017145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122967520-A-G

http://identifiers.org/hco/3/GRCh38#45017810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122967966-A-C

45018245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968282-T-C

45018315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968325-A-T

45018413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968406-G-A

45018418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968411-A-G

45018499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968460-A-G

45018594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968557-C-T

45018617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968580-G-A

45018617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968580-G-T

45018759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968690-G-A

45018867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968796-T-C

45018915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122968865-G-T

45020594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976547-A-G

45020620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976572-T-C

45020621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976573-G-A

45020688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976639-C-G

45020746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976701-A-T

45020760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976715-G-C

http://identifiers.org/hco/3/GRCh38#45020762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122976717-C-A

45020762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976717-C-T

45020807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976751-C-T

45020895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122976829-A-T

45021511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122977479-G-A

http://identifiers.org/hco/3/GRCh38#45021680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122977664-C-A

45025240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122979273-G-A

http://identifiers.org/hco/3/GRCh38#45025285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122979324-A-C

45025456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122979425-A-G

45025565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122979516-C-T

45025579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122979531-C-T

45025681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122979633-G-A

http://identifiers.org/hco/3/GRCh38#45026034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122979795-A-C

45026040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122979801-G-T

45026113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122979874-A-G

45026240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980011-G-A

45026240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980011-G-T

http://identifiers.org/hco/3/GRCh38#45026255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122980026-A-C

http://identifiers.org/hco/3/GRCh38#45026286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122980058-C-A

45026286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980058-C-T

45026292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980064-G-T

45026361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122980107-G-T

45026421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 122980167-C-T

45026463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 122980209-C-T

45026484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980242-A-G

45026484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980242-A-T

45026517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980300-C-T

45026547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980329-T-C

45026547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980329-T-G

http://identifiers.org/hco/3/GRCh38#45026563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122980346-C-A

45026563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980346-C-T

45026594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980376-G-T

45026672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980449-T-G

http://identifiers.org/hco/3/GRCh38#45026681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122980458-C-A

45027199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980862-G-A

45027199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980862-G-C

45027293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122980924-G-C

45029498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982317-A-G

45029533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982353-T-C

45029647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982461-T-C

45029715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982514-C-G

45029768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982564-C-T

45029945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982753-G-A

http://identifiers.org/hco/3/GRCh38#45030010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122982789-C-A

45030010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982789-C-T

http://identifiers.org/hco/3/GRCh38#45030015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122982794-C-A

45030015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982794-C-T

45030059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982835-G-A

45030059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982835-G-T

45030080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982855-A-G

45030080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122982855-A-T

45030211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122982975-T-A

45030234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122982979-T-C

http://identifiers.org/hco/3/GRCh38#45030308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122983055-C-A

45030308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983055-C-G

http://identifiers.org/hco/3/GRCh38#45030326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122983069-C-A

45030326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983069-C-T

http://identifiers.org/hco/3/GRCh38#45030685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122983324-C-A

45030691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983330-G-A

45030691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983330-G-T

45030725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983377-T-A

45030725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983377-T-C

45030728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983380-A-G

45030822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122983477-T-G

45030855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122983510-G-A

45030855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122983510-G-T

45030924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 122983579-G-A

45030924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 122983579-G-C

45030924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 122983579-G-T

45030955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983608-G-A

45030955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983608-G-C

http://identifiers.org/hco/3/GRCh38#45030984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122983638-C-A

45030984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983638-C-T

45031039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983660-T-A

45031039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983660-T-C

45031074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983680-G-A

45031074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983680-G-T

http://identifiers.org/hco/3/GRCh38#45031077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122983683-C-A

45031077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983683-C-T

45031138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983744-C-T

45031315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122983899-C-T

http://identifiers.org/hco/3/GRCh38#45035434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122985730-A-C

45035434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122985730-A-G

http://identifiers.org/hco/3/GRCh38#45035469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122985762-C-A

45035469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122985762-C-G

45035469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122985762-C-T

45035564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 122985852-G-A

45035564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 122985852-G-C

http://identifiers.org/hco/3/GRCh38#45035600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122985888-C-A

45035600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122985888-C-T

http://identifiers.org/hco/3/GRCh38#45035702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122985990-C-A

45035702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122985990-C-G

45035702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122985990-C-T

45035961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122986303-G-A

45035961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122986303-G-C

45035961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122986303-G-T

45035973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986315-G-A

45035973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986315-G-C

45035973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986315-G-T

45035974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986326-G-A

45035974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986326-G-T

http://identifiers.org/hco/3/GRCh38#45035983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122986335-A-C

45035983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986335-A-G

45035983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986335-A-T

45035988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986340-G-C

http://identifiers.org/hco/3/GRCh38#45035996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122986412-C-A

45035996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28112
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122986412-C-T