93992854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973695-T-C

93992863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973686-T-A

93992870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973679-A-G

http://identifiers.org/hco/1/GRCh38#93992884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121973665-C-A

93992924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973626-G-A

93992924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973626-G-T

93992943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973607-T-C

http://identifiers.org/hco/1/GRCh38#93992955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121973595-C-A

93992957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973593-G-A

93992957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973593-G-C

93992980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973579-C-G

93992980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973579-C-T

93993006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973560-T-G

93993048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973519-A-G

93993053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973514-G-C

93993053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973514-G-T

http://identifiers.org/hco/1/GRCh38#93993089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121973479-C-A

93993089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973479-C-G

93993089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973479-C-T

93993107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973461-T-G

93993134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973434-T-C

93993137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973431-A-T

93993164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973408-T-C

93993194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3 prime UTR variant
orthologous variants: 121973378-C-T

http://identifiers.org/hco/1/GRCh38#93993260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121973311-A-C

93993260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121973311-A-G

http://identifiers.org/hco/1/GRCh38#93993363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121973223-C-A

93993550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121973022-A-T

93993605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121972773-A-G

93993820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121972546-G-T

93993852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121972514-G-A

93993974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121972398-T-A

93994035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121972221-A-T

93994044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121972045-A-G

93994196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121971897-C-T

93994427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121971668-A-G

93994804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121971273-C-G

93995209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121970809-A-T

93995356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121970657-C-T

93995494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121970510-G-A

93995522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121970486-G-A

93995614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121970383-C-T

93995793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121970218-C-G

93995801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121970194-C-T

93995864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121970033-C-T

93995962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969927-G-A

93995962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969927-G-T

93995963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969926-T-C

93995963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969926-T-G

93996018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969898-G-A

93996018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969898-G-T

93996065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969850-A-G

93996080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969836-G-A

93996080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969836-G-C

93996080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969836-G-T

93996120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: stop gained
orthologous variants: 121969796-G-A

93996120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: synonymous variant
orthologous variants: 121969796-G-T

http://identifiers.org/hco/1/GRCh38#93996161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121969755-C-A

93996227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969695-A-T

93996246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969676-A-G

http://identifiers.org/hco/1/GRCh38#93996258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121969656-C-A

93996271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969643-C-T

93996293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969621-A-G

93996314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969600-T-C

93996316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969598-G-T

http://identifiers.org/hco/1/GRCh38#93996324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121969590-C-A

93996324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969590-C-T

http://identifiers.org/hco/1/GRCh38#93996343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121969581-C-A

93996343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969581-C-T

93996688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969252-A-T

http://identifiers.org/hco/1/GRCh38#93996695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121969245-C-A

93996695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969245-C-T

93996734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969178-C-T

93996828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969122-A-G

93996853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121969110-G-A

93997576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967942-G-C

93997576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967942-G-T

93997696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967837-G-T

93997717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967816-T-C

93997749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967784-G-T

93997819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967710-A-G

93997958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121967578-G-A

93997958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121967578-G-T

93998567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967317-T-G

93998580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967304-A-G

93998584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967300-A-T

93998598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121967286-A-G

93999638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121965861-C-T

http://identifiers.org/hco/1/GRCh38#93999684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121965815-C-A

94000221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121965264-C-T

94000239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121965249-G-A

94000321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121965158-G-A

94000381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121965113-T-C

94000445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121965045-A-G

94000501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964988-A-G

94000631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964856-C-T

94000641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964846-T-C

94000655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964832-G-A

94000714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964784-A-T

94000748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964751-G-C

94000748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964751-G-T

http://identifiers.org/hco/1/GRCh38#94000750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121964749-A-C

94000774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964730-G-T

94000811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964693-G-C

94000811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964693-G-T

94000812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964692-G-A

94000812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964692-G-C

http://identifiers.org/hco/1/GRCh38#94000896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121964608-A-C

94000899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121964605-C-G

94000899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121964605-C-T

94000962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964537-G-A

94000962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964537-G-T

http://identifiers.org/hco/1/GRCh38#94000974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121964520-A-C

94000974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964520-A-G

http://identifiers.org/hco/1/GRCh38#94000980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121964514-C-A

94001026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121964468-C-T

94001131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964361-G-A

94001131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964361-G-T

94001137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964355-G-A

94001137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964355-G-T

94001139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964353-T-A

94001139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964353-T-C

94001147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964345-G-T

94001148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964344-G-T

94001211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964303-G-A

94001211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964303-G-T

94001265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964253-G-C

94001282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964237-A-G

94001413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964070-G-T

94001422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121964061-C-T

http://identifiers.org/hco/1/GRCh38#94001508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121963980-C-A

94001508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963980-C-T

http://identifiers.org/hco/1/GRCh38#94001557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121963895-C-A

94001570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963882-C-T

94001596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963857-G-A

94001596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963857-G-T

http://identifiers.org/hco/1/GRCh38#94001597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121963856-A-C

94001597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963856-A-G

94001651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963819-G-A

94001651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963819-G-T

94001722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963773-G-A

94001722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963773-G-T

94001762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963761-G-T

94001780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963744-G-A

94001780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963744-G-C

94001780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963744-G-T

http://identifiers.org/hco/1/GRCh38#94001813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121963711-C-A

94001813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963711-C-G

94001835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963693-G-A

http://identifiers.org/hco/1/GRCh38#94001838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121963690-C-A

94001838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963690-C-G

94001838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121963690-C-T

94001949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121963583-G-A

94001949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121963583-G-C

94001949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121963583-G-T

94002020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963513-G-T

94002064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963465-T-C

94002075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963454-A-T

94002089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963440-G-A

http://identifiers.org/hco/1/GRCh38#94002098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121963439-C-A

http://identifiers.org/hco/1/GRCh38#94002132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121963403-C-A

94002132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963403-C-G

94002132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963403-C-T

94002227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963335-T-C

94002365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963231-C-T

94002368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963228-G-A

94002427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121963165-A-G

http://identifiers.org/hco/1/GRCh38#94005250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121960614-C-A

94005250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960614-C-G

94005250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960614-C-T

94005269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960595-A-G

94005269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960595-A-T

94005301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960565-A-G

94005327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960544-G-T

94005403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121960474-A-G

94005404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121960473-C-T

94005493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121960384-T-C

94005640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960240-A-T

http://identifiers.org/hco/1/GRCh38#94005664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121960223-C-A

94005664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960223-C-T

94005666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960221-A-T

http://identifiers.org/hco/1/GRCh38#94005694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121960206-C-A

94005715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960191-G-A

94005715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960191-G-T

94005729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960179-G-A

94005729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121960179-G-C

94005964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959938-G-A

http://identifiers.org/hco/1/GRCh38#94006160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121959753-A-C

http://identifiers.org/hco/1/GRCh38#94006161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121959752-C-A

94006163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959750-T-C

94006200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959711-G-T

94006257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959649-C-G

94006325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959581-A-G

94006426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959488-T-A

94006461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959459-T-C

94006496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959445-T-A

94006838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959128-T-G

94006876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121959097-T-C

94007023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121958157-A-G

94007161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121958011-A-G

94007197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957979-G-A

94007208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957968-C-T

94007317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957860-A-G

94007353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957825-G-A

94007443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957738-A-G

http://identifiers.org/hco/1/GRCh38#94007468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121957712-C-A

94007468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957712-C-T

94007529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957650-C-T

94007574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957606-C-T

http://identifiers.org/hco/1/GRCh38#94007593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121957582-C-A

94007593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957582-C-T

94007658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121957517-C-T

94007788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957387-T-A

94007841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957344-G-C

94007841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957344-G-T

94007868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121957316-G-T

94008031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956740-G-C

94008053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956722-A-G

94008229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956576-A-G

94008242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121956563-G-A

94008242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121956563-G-T

http://identifiers.org/hco/1/GRCh38#94008245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121956560-C-A

94008245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121956560-C-T

94008334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956471-C-T

94008456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956327-C-G

94008464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956319-G-A

http://identifiers.org/hco/1/GRCh38#94008556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121956227-A-C

94008655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956147-G-T

94008716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956111-A-G

http://identifiers.org/hco/1/GRCh38#94008740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121956078-C-A

94008740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121956078-C-T

94008761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121956058-T-A

94008827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121955992-T-A

94008845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121955974-A-G

94008904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955915-G-T

94008920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955896-G-T

94008921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955895-G-A

94008921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955895-G-T

http://identifiers.org/hco/1/GRCh38#94008924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121955892-C-A

94008929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955887-C-G

94008929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955887-C-T

http://identifiers.org/hco/1/GRCh38#94008941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121955875-C-A

94009346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955500-A-G

http://identifiers.org/hco/1/GRCh38#94009394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121955455-A-C

94009662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955203-G-A

94009662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121955203-G-T

94009849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121953023-G-A

http://identifiers.org/hco/1/GRCh38#94010082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121952834-A-C

http://identifiers.org/hco/1/GRCh38#94010251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121952661-C-A

94010251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121952661-C-T

94010309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121952608-G-A

94010355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121952539-C-G

94010355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121952539-C-T

94010744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121952148-G-A

http://identifiers.org/hco/1/GRCh38#94010760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121952132-C-A

94010760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121952132-C-T

94010762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121952130-T-C

94010764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121952128-A-G

94010941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121951933-C-T

94010953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121951921-C-T

94010963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121951911-C-T

94011032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121951858-A-G

http://identifiers.org/hco/1/GRCh38#94011045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121951841-C-A

94011045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121951841-C-T

94011230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121951636-C-T

94011417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121951447-G-A

94011417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121951447-G-T

94013715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121950787-G-A

94013971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121950542-T-C

94014523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121950152-G-A

94014622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121950053-G-T

94014726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121949949-C-G

94014743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121949932-T-A

94014939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121949777-T-C

94015267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121949442-C-T

94015520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121949187-T-C

http://identifiers.org/hco/1/GRCh38#94015603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121949141-C-A

94015603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121949141-C-G

94015629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121949116-G-A

94015629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121949116-G-T

94015633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121949112-G-A

94015633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121949112-G-T

http://identifiers.org/hco/1/GRCh38#94015640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121949105-C-A

94015640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121949105-C-T

94015660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121949085-T-G

94015723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121949055-G-A

94015723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121949055-G-T

http://identifiers.org/hco/1/GRCh38#94015759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121949019-C-A

94015759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: synonymous variant
orthologous variants: 121949019-C-T

94015832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121948946-C-T

94015838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121948940-C-T

94015880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121948901-T-A

http://identifiers.org/hco/1/GRCh38#94016066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121948741-C-A

94016066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121948741-C-T

94016087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121948719-A-G

94016285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121948520-G-A

http://identifiers.org/hco/1/GRCh38#94016314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121948482-C-A

94016333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121948463-G-A

94016394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121948424-C-T

94017747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121945647-G-C

94017759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121945635-A-G

94017825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121945582-A-G

94017968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121945442-C-T

http://identifiers.org/hco/1/GRCh38#94018039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121945371-A-C

94018095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121945315-T-C

94018399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944810-G-A

94018426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944786-G-A

94018426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944786-G-T

94018514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944698-A-G

94018514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944698-A-T

94018520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944692-G-T

94018550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944659-A-G

94018550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944659-A-T

94018626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121944584-G-A

94018796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121943600-G-C

94018870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121943538-A-G

94018870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121943538-A-T

94018901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121943508-C-T

http://identifiers.org/hco/1/GRCh38#94019012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121943125-C-A

94019073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121943082-G-T

http://identifiers.org/hco/1/GRCh38#94019086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121943069-C-A

94019132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121943023-G-A

94019213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121942930-G-A

94019408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121942826-G-A

94019408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121942826-G-T

94019431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121942806-G-A

94019431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121942806-G-T

94019549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121942725-G-T

94019823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121942477-A-G

http://identifiers.org/hco/1/GRCh38#94019853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121942446-A-C

94020065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121942245-C-T

94020719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121942035-C-T

94020799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941959-A-G

94020801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941957-A-G

94020882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941889-T-C

94021102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941680-G-T

94021106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941676-G-T

94021126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941656-T-C

94021190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941585-A-G

94021294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121941492-G-A

94021294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121941492-G-T

94021501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941264-G-A

94021501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941264-G-C

94021501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941264-G-T

94021537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941236-G-T

94021548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941228-G-A

94021548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941228-G-T

94021750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941043-T-A

94021753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941040-T-C

94021754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121941039-T-G

94021872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121940924-G-T

94021912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121940884-G-A

94021912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121940884-G-T

94021915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121940881-G-A

94021915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121940881-G-T

94021964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121940833-C-G

94022021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121940776-T-C

94022031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121940767-A-G

94022038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121940760-A-G

94022464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121938439-A-G

94022466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121938437-C-T

94022532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121938371-T-C

94022548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121938356-C-G

94022795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937830-T-C

94022875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937750-C-T

94023038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937522-A-G

94023446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937019-G-A

94023446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937019-G-T

94023448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937017-A-G

94023448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937017-A-T

94023462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937003-G-A

94023462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937003-G-C

94023462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121937003-G-T

94023471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936994-T-C

94023481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936984-T-C

94023522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936955-G-T

http://identifiers.org/hco/1/GRCh38#94023526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121936951-C-A

94023559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936918-G-A

http://identifiers.org/hco/1/GRCh38#94023567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121936909-C-A

94023612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936862-A-G

http://identifiers.org/hco/1/GRCh38#94023776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121936692-C-A

94023972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936552-G-A

94024100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936400-A-G

94024100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936400-A-T

94024103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936397-C-T

94024115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936385-G-A

94024125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121936375-C-T

http://identifiers.org/hco/1/GRCh38#94024352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121936147-A-C

http://identifiers.org/hco/1/GRCh38#94024560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121935941-C-A

94024756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935601-G-C

94024774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935583-A-G

94024790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935567-C-T

94024846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935532-T-C

94024903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935480-A-G

94024903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935480-A-T

94024906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935477-T-C

94025102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935293-T-C

94025141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935256-A-T

94025165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935233-C-T

http://identifiers.org/hco/1/GRCh38#94025169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121935229-A-C

94025169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935229-A-G

94025235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935159-T-A

94025235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935159-T-C

94025297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935103-G-A

94025314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935088-A-G

94025382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121935009-T-C

94025405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121934986-T-A

94025416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121934976-A-G

94025429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121934963-T-A

http://identifiers.org/hco/1/GRCh38#94025465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121934941-C-A

94025520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121934933-C-T

94025559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121934914-T-C

94025583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121934911-T-C

94025605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934889-T-C

94025610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934884-G-A

94025610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934884-G-C

94025610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934884-G-T

94025620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934875-G-T

94025713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934870-C-T

94025825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934852-G-A

94025826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934851-G-A

94025830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934847-T-A

94025838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934839-G-A

94025930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121934761-C-T

94026042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121934688-G-A

94026150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121934558-G-T

http://identifiers.org/hco/1/GRCh38#94026256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121934479-C-A

94026291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934456-G-A

94026327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934420-T-G

94026550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121934254-C-T

94027733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121933434-T-C

94027961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121933154-G-A

94028060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121933056-T-C

94028334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121932787-G-A

94028441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121932689-G-A

94029436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121932266-G-T

http://identifiers.org/hco/1/GRCh38#94029487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121932215-C-A

94029487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: synonymous variant
orthologous variants: 121932215-C-T

94029582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121932120-G-C

94029582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121932120-G-T

94029636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121932066-T-A

94029636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121932066-T-C

94029755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931943-T-A

94029755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931943-T-C

94029757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931941-T-C

94029757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931941-T-G

94029809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931892-C-T

94029818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931884-G-C

94030309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931422-G-T

http://identifiers.org/hco/1/GRCh38#94030345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121931380-C-A

94030345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931380-C-T

94030351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931374-G-A

94030351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931374-G-C

94030351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931374-G-T

94030372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931359-G-A

94030372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931359-G-T

94030485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121931258-T-C

94030540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931203-G-T

94030566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931162-C-G

94030566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931162-C-T

94030631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931102-G-A

94030641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931092-G-A

94030641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931092-G-T

http://identifiers.org/hco/1/GRCh38#94030642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121931091-C-A

94030642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931091-C-T

94030660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931073-A-G

94030673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931060-G-T

http://identifiers.org/hco/1/GRCh38#94030676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121931057-C-A

94030676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931057-C-T

http://identifiers.org/hco/1/GRCh38#94030720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121931014-C-A

94030720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121931014-C-T

94031152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121930573-C-T

94031217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121930503-G-A

94031217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121930503-G-T

94031222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121930499-C-T

http://identifiers.org/hco/1/GRCh38#94031227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121930494-A-C

94031255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121930466-T-C

94031900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121928789-C-G

94032010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121928682-G-T

http://identifiers.org/hco/1/GRCh38#94032137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121928563-C-A

94032137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121928563-C-T

94032138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121928562-T-A

94035129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121927944-G-A

94035354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121927744-G-C

94035395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121927703-C-T

94035765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121927369-G-A

94035770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121927364-T-C

94035790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121927343-C-T

94035920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121927260-T-C

94035958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121927222-C-T

http://identifiers.org/hco/1/GRCh38#94036038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121927135-A-C

94036259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926908-C-T

94036260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926907-T-C

94036291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926887-A-G

94036320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926860-G-A

94036323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926857-T-C

94036802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926689-A-G

94036807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926684-G-A

94036885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926618-G-A

94036885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926618-G-T

http://identifiers.org/hco/1/GRCh38#94037006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121926510-C-A

94037006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926510-C-T

94037061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926459-C-G

94037061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121926459-C-T

94037285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121926236-T-A

94037285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121926236-T-C

94037285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121926236-T-G

94037354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121926167-G-A

http://identifiers.org/hco/1/GRCh38#94037437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121926074-C-A

http://identifiers.org/hco/1/GRCh38#94037626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121925479-C-A

94037627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121925478-A-G

94038138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121925042-G-A

94038138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121925042-G-C

94038138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121925042-G-T

94038347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121924945-C-T

94038348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121924944-G-A

94038675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121924641-C-G

94038899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121924434-C-G

94039129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121924242-G-C

http://identifiers.org/hco/1/GRCh38#94039899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121923184-C-A

94039899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121923184-C-G

http://identifiers.org/hco/1/GRCh38#94039968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121923119-C-A

94039987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121923100-C-T

94040015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121923075-A-G

94040034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121923056-A-T

94040045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 121923045-T-A

94040076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, undefined
orthologous variants: 121923014-C-G

94040076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, undefined
orthologous variants: 121923014-C-T

94040136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121922954-G-C

94040136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121922954-G-T

http://identifiers.org/hco/1/GRCh38#94040186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121922904-C-A

94040186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922904-C-T

94040208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922882-G-A

94040208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922882-G-T

http://identifiers.org/hco/1/GRCh38#94040260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121922829-C-A

94040260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121922829-C-T

94040840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922296-A-T

http://identifiers.org/hco/1/GRCh38#94040865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121922271-A-C

http://identifiers.org/hco/1/GRCh38#94040948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121922202-C-A

94040954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922196-C-T

94041084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922072-T-C

http://identifiers.org/hco/1/GRCh38#94041113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121922047-C-A

94041113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922047-C-G

94041113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922047-C-T

94041116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922044-G-A

94041124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922036-G-T

http://identifiers.org/hco/1/GRCh38#94041150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121922010-C-A

94041150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922010-C-G

94041150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121922010-C-T

http://identifiers.org/hco/1/GRCh38#94041297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121921877-A-C

94041297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121921877-A-G

94041297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121921877-A-T

94041348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121921826-T-C

94041789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121921364-G-C

94041824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121921340-G-A

94042649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920715-T-A

94042649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920715-T-C

94042650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920714-G-A

94042650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920714-G-T

94042808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121920559-G-C

94042808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121920559-G-T

94042829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121920538-T-C

94042917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920444-C-T

94042929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920432-G-C

94042937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920424-G-T

http://identifiers.org/hco/1/GRCh38#94042960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121920401-C-A

94042960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920401-C-T

94042962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920399-G-C

http://identifiers.org/hco/1/GRCh38#94043009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121920352-C-A

94043009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920352-C-T

94043014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920347-T-C

94043022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920336-G-A

94043022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920336-G-T

94043087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920273-T-C

http://identifiers.org/hco/1/GRCh38#94043234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121920067-C-A

94043234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920067-C-T

94043240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920005-G-T

94043243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121920002-G-T

94043278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919965-G-A

94043282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919961-T-G

94043304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919939-C-T

94043311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919932-C-T

94043322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919921-C-T

94043365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121919878-T-C

94043377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121919866-C-T

http://identifiers.org/hco/1/GRCh38#94043499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121919744-A-C

94043499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919744-A-T

94043554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919689-G-T

94043591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919656-G-A

94043669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919579-T-C

94043738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919516-T-A

94043754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919500-T-C

94043807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919265-A-G

94043846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919226-G-C

94043904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121919175-A-G

94044563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917427-G-A

94044581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917409-G-A

94044581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917409-G-T

94044582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917408-A-T

94044770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917180-G-A

94044793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917158-G-A

http://identifiers.org/hco/1/GRCh38#94044812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121917137-C-A

94044812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917137-C-G

94044812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917137-C-T

94044823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917126-C-T

94044849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121917100-C-G

94045000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121916932-T-A

94045231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121916559-T-C

http://identifiers.org/hco/1/GRCh38#94045655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121916111-A-C

94045655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 121916111-A-G

94045725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 121916048-G-T

94045781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 121915992-C-G

94045795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 121915980-G-A

94045795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 121915980-G-C

94045810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 121915965-T-A

94045810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 121915965-T-C

94045832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 121915939-A-G

94045931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant
orthologous variants: 121915831-C-T

94045932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121915830-G-T

94045934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant
orthologous variants: 121915828-G-A

94045934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant
orthologous variants: 121915828-G-C

94045934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant
orthologous variants: 121915828-G-T

http://identifiers.org/hco/1/GRCh38#94046007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121915763-A-C

94046007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915763-A-T

94046062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915723-T-C

94046840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915529-G-T

http://identifiers.org/hco/1/GRCh38#94046867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121915499-C-A

94046867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915499-C-T

http://identifiers.org/hco/1/GRCh38#94046901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121915470-C-A

94046901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915470-C-T

94046940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121915431-C-T

http://identifiers.org/hco/1/GRCh38#94047129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121915235-A-C

94047130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915234-T-C

94047170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915198-T-C

94047197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915171-C-T

94047221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915154-G-T

http://identifiers.org/hco/1/GRCh38#94047228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121915147-A-C

94047228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121915147-A-G

94047449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914932-T-C

94047471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914917-T-C

94047862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914702-C-G

94047862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914702-C-T

94047874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914690-C-T

94047894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914660-C-T

94047995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914560-G-A

94048300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914316-G-A

94048302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914314-G-A

94048520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914107-C-T

94048601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121914026-G-A

94048726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913913-A-T

http://identifiers.org/hco/1/GRCh38#94048747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121913892-C-A

94048833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913815-T-C

94048834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913814-C-T

94048882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121913752-G-A

94048981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913653-T-A

94049025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913627-G-A

http://identifiers.org/hco/1/GRCh38#94049035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121913617-A-C

94049035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913617-A-G

94049035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913617-A-T

94049056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913596-T-C

94049077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913505-T-A

94049077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913505-T-C

94049081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913501-A-T

94049088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913494-G-A

94049088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913494-G-T

94049107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913475-A-G

94049347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913274-C-T

94049400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913223-C-T

94049419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913211-T-A

94049427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121913203-C-T

94049667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912965-G-A

94049755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912879-A-G

94049765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912869-C-T

94049845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912801-C-T

http://identifiers.org/hco/1/GRCh38#94049851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121912790-A-C

94049917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912726-G-A

94050018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912635-C-T

http://identifiers.org/hco/1/GRCh38#94050025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121912627-A-C

94050051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912607-C-T

94050155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912529-T-C

94050453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121912225-G-A

http://identifiers.org/hco/1/GRCh38#94050522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121912157-A-C

94050726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121911912-T-C

94050790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121911797-G-A

94050790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121911797-G-T

94050980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121911365-A-T

94051509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121910853-G-A

94051548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121910817-G-A

94051548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121910817-G-T

94051659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121910341-T-G

94051716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121910288-T-G

94051798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121910218-A-G

94051798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121910218-A-T

94051845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121910167-G-T

94051894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121910115-T-C

94052083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121909918-G-C

94052120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121909880-A-G

94052158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121909843-C-T

94054092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121907669-T-C

94054359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121907428-T-G

94054374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121907416-T-A

94054376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121907414-G-A

94054444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121907345-T-C

94054614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121907194-A-G

94054614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121907194-A-T

94054950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121906404-G-A

94054999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121906358-A-G

94055002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121906355-C-T

94055067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121906278-C-G

94055067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121906278-C-T

94055179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121906149-A-T

http://identifiers.org/hco/1/GRCh38#94055301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121906027-C-A

94055301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: synonymous variant
orthologous variants: 121906027-C-T

94055308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121906020-A-G

94055370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905975-A-G

94055408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905932-A-G

94055422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905920-T-C

94055423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905919-T-G

94055438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905904-G-A

94055438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905904-G-T

94055514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905372-G-C

94055521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905365-T-C

94055674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121905186-C-T

http://identifiers.org/hco/1/GRCh38#94056100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121904802-C-A

94056157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904746-G-C

94056476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904436-G-A

94056476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904436-G-T

94056484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904428-T-C

94056522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904392-G-A

94056522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904392-G-T

94056652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121904279-G-A

94056652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121904279-G-T

94056653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant
orthologous variants: 121904278-A-T

94056739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121904192-G-A

94056840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904090-T-C

94056869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904061-C-T

http://identifiers.org/hco/1/GRCh38#94056878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121904052-A-C

94056901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121904027-C-T

http://identifiers.org/hco/1/GRCh38#94056973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121903952-C-A

94056973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121903952-C-T

94057618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121902116-A-G

94057684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121902061-T-C

94057773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121901999-C-T

94058027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121901517-T-C

http://identifiers.org/hco/1/GRCh38#94058703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121901244-A-C

94058781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121901198-C-G

94059400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121900595-A-G

http://identifiers.org/hco/1/GRCh38#94059428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121900567-C-A

94059428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121900567-C-T

94059544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121900456-A-G

94059656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 121900371-T-C

94059665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121900362-T-C

94059839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121900208-G-T

94060049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899679-T-C

94060103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899621-C-T

94060104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899620-T-G

94060267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899461-C-T

94060407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899308-G-T

http://identifiers.org/hco/1/GRCh38#94060414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121899307-C-A

94060415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899306-T-G

94060417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899304-G-A

94060417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899304-G-T

94060488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899227-A-G

94060488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121899227-A-T

94060583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121899131-A-T

http://identifiers.org/hco/1/GRCh38#94060586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121899128-C-A

94060607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 121899107-C-T

94060709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 121899005-C-T

94060765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121898949-G-A

94060771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898943-G-A

94060771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898943-G-T

94060788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898930-T-A

94060788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898930-T-G

94060907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898815-G-A

94060907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898815-G-T

94061337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898577-C-T

94061338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898576-C-T

94061352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898561-G-A

94061352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121898561-G-T

http://identifiers.org/hco/1/GRCh38#94061391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121898522-C-A

94061574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121898336-T-C

http://identifiers.org/hco/1/GRCh38#94061662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121898248-C-A

94061662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121898248-C-T

94061741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121898182-T-A

94061741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121898182-T-C

94061743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121898180-C-T

94061988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897815-A-G

94062041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897762-T-C

94062070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121897732-G-A

94062156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121897644-T-C

94062293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897503-C-T

94062365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897430-C-T

94062389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897423-T-A

94062395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897417-C-T

http://identifiers.org/hco/1/GRCh38#94062439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121897373-A-C

94062439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897373-A-G

94062439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897373-A-T

http://identifiers.org/hco/1/GRCh38#94062447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121897365-C-A

94062481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897332-G-T

http://identifiers.org/hco/1/GRCh38#94062522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121897296-A-C

94062641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: stop gained
orthologous variants: 121897193-G-A

94062641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121897193-G-C

94062641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121897193-G-T

94062655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121897179-G-A

94062706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121897128-T-A

94062706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121897128-T-C

http://identifiers.org/hco/1/GRCh38#94062812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121897020-C-A

94062812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121897020-C-G

94062872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896947-A-G

94062872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896947-A-T

http://identifiers.org/hco/1/GRCh38#94062895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121896868-C-A

94062895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896868-C-T

94062967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896681-T-C

94062967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896681-T-G

94062970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896678-T-C

94063058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896576-T-C

94063181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121896458-G-A

94063286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, undefined
orthologous variants: 121896353-T-C

94063319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: splice acceptor variant
orthologous variants: 121896320-T-G

94063434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896221-G-A

94063434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896221-G-T

94063436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121896219-G-T

94063448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121896207-T-A

94063448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121896207-T-G

94063475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121896180-T-C

94064543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121895219-C-T

94064895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121894905-A-G

94064937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121894887-G-C

94065122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121894732-G-A

http://identifiers.org/hco/1/GRCh38#94065268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121894564-C-A

94065268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121894564-C-T

94065313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121894343-C-T

94065417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121894235-A-G

94065720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121894015-G-A

94065720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121894015-G-C

94066096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121893744-C-T

94066120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121893719-G-C

94066154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121893679-G-A

94066637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121892647-C-G

94066637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121892647-C-T

94066707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121892578-G-A

http://identifiers.org/hco/1/GRCh38#94066718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121892556-C-A

94066798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121892485-C-G

94067203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121892042-A-G

94067268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121891944-C-T

94067281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121891932-C-T

94067378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121891851-A-G

94067475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121891756-A-G

94067475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121891756-A-T

94067512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121891717-C-T

94067593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121891649-C-T

94068088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121891045-T-C

94068131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121890999-C-T

94068228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121890930-G-T

94068505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121890693-A-G

94068614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121890590-A-G

94068672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121890537-G-C

94068785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121890456-C-T

94069097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121890193-G-A

94069130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121890176-C-G

94069146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121890160-T-C

94069309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121889998-G-C

94069493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121889832-G-A

94069493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121889832-G-C

94069778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121889580-A-T

94069835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121889537-G-A

94070511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121887578-C-T

94070651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121887417-T-C

94070695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121887373-C-T

94070732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121887335-G-T

94070746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121887322-G-A

94070760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121887308-G-A

94071390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121887039-T-C

94071481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121886957-T-A

94071481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121886957-T-G

94071578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121886856-A-G

94071656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121886786-C-T

94071730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121886742-C-T

94072064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121886433-A-T

94072672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121885848-G-C

http://identifiers.org/hco/1/GRCh38#94073299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121884145-C-A

94073395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121884062-C-T

94073580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883853-A-G

94073752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883687-T-C

94073848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883482-T-G

94073900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883449-C-T

94073919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883430-G-A

94073951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883393-G-A

94074021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883337-T-C

94074058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883318-C-T

94074095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883288-C-G

94074099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883284-C-G

94074099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883284-C-T

http://identifiers.org/hco/1/GRCh38#94075406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121883194-C-A

94075457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883151-C-T

94075519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121883082-G-C

94076235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121882286-G-A

94076976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121881821-C-G

94076976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121881821-C-T

94077042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121881754-C-T

94077094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121881700-T-C

94077115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121881680-A-G

94077486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121881319-G-C

94077581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121881256-G-T

http://identifiers.org/hco/1/GRCh38#94078108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121880742-A-C

94078108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880742-A-T

94078466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880401-T-G

94078468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880399-G-A

94078468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880399-G-C

94078468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880399-G-T

94078506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880361-T-C

94078506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880361-T-G

http://identifiers.org/hco/1/GRCh38#94078596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121880316-C-A

94078596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121880316-C-T

http://identifiers.org/hco/1/GRCh38#94078597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121880315-A-C

94078656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121880256-G-A

94078656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121880256-G-C

http://identifiers.org/hco/1/GRCh38#94078845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121880000-A-C

94078845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880000-A-G

94078845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121880000-A-T

94079175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121879550-A-G

94079249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121879472-T-A

94079249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121879472-T-C

94079257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121879464-A-G

94079257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121879464-A-T

http://identifiers.org/hco/1/GRCh38#94079302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121879340-A-C

94079328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 121879314-C-T

94079336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 121879306-T-C

94079392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121879250-G-C

94079393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121879249-C-G

94079393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121879249-C-T

94079467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121879175-A-G

94079467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121879175-A-T

94079651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121878986-T-C

94079820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121878774-T-C

94080245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121878471-T-C

94080656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121877561-A-G

94080787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121877311-C-G

94080787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121877311-C-T

94080792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121877302-A-G

http://identifiers.org/hco/1/GRCh38#94080811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121877236-C-A

http://identifiers.org/hco/1/GRCh38#94080829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121877220-C-A

94080830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121877219-A-G

94080831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121877218-T-C

94080831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121877218-T-G

94080890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121877161-C-G

94080890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121877161-C-T

94081685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121876539-T-G

94081985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121876228-G-A

94082144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121876063-A-G

94082178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121876029-T-C

94082335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875877-C-G

94082335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875877-C-T

94082337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875875-A-G

94082403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875809-T-C

94082530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875471-T-G

94082649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875351-G-T

94082686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875302-C-T

94082742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875242-T-C

http://identifiers.org/hco/1/GRCh38#94082791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121875193-C-A

94082920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875067-A-G

94082927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121875060-A-G

94082980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121874995-C-T

94083211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121874789-G-A

94083211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121874789-G-T

94083218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121874782-G-T

94083264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121874737-T-C

94083264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121874737-T-G

94083288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121874713-C-T

94083309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121874687-A-G

94083575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121873913-A-G

94083585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121873903-T-G

94090858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873686-G-T

94090859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873685-G-C

94090859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873685-G-T

94091047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873519-C-T

94091084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873487-C-T

94091117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873455-G-A

94091152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873421-T-C

94091156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873417-G-A

94091156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873417-G-T

94091183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873386-T-G

94091319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873041-A-G

94091333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121873029-T-C

94091371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121872992-A-G

94091693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121872730-C-T

94091838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121872580-G-T

94092154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121872311-A-G

94092243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121872222-T-C

94092718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121871719-C-T

94092803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121871459-T-G

94093300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121869305-T-C

94093310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121869295-C-T

94093417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121869187-T-C

94093421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121869183-G-C

94093664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868940-A-T

94093827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868792-T-A

94093833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868786-T-C

94093867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868755-G-A

94094002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868544-T-G

94094067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868454-A-G

94094106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868387-T-A

94094186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868305-T-C

94094256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121868233-G-A

94094616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121867878-G-C

http://identifiers.org/hco/1/GRCh38#94094630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121867865-C-A

94094790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121867702-G-A

http://identifiers.org/hco/1/GRCh38#94094832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121867662-A-C

94094979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121867463-G-A

94094979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121867463-G-T

http://identifiers.org/hco/1/GRCh38#94094996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121867430-C-A

94095023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121867412-G-A

94095110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121867327-G-A

94095110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121867327-G-C

94095829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866508-A-G

94095836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866472-G-T

http://identifiers.org/hco/1/GRCh38#94095923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121866386-A-C

94095967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866353-C-G

94095967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866353-C-T

http://identifiers.org/hco/1/GRCh38#94095977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121866343-C-A

94096030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866290-C-G

http://identifiers.org/hco/1/GRCh38#94096035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121866285-C-A

94096035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866285-C-G

94096041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866279-T-G

94096132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866211-T-C

94096141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121866194-C-G

94097139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121864575-A-G

94097546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863696-A-G

94097552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863690-T-A

94097552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863690-T-C

94097610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863644-A-G

http://identifiers.org/hco/1/GRCh38#94098133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121863510-A-C

94098163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863482-G-T

94098343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863314-A-G

94098349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863309-T-A

94098356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863302-C-T

94098444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863086-T-C

94098477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863069-G-A

94098477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121863069-G-C

http://identifiers.org/hco/1/GRCh38#94098796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121862807-C-A

94098796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 121862807-C-T

94098854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: synonymous variant
orthologous variants: 121862749-G-A

94098879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121862724-G-A

94098889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121862714-C-T

94099023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121862580-C-T

94099032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121862571-A-G

94099196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121862256-C-G

94099322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121862124-G-A

94099527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121861706-C-T

94099651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121861564-G-A

94099651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121861564-G-T

94099863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121861202-G-A

94099937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121861113-T-C

94099957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121861093-C-T

94100369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121859273-C-G

94100640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121859058-C-T

94100697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121858990-G-A

94100697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121858990-G-C

94100775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121858914-A-G

94100779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121858910-A-G

http://identifiers.org/hco/1/GRCh38#94101109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121858597-C-A

94101418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121858320-C-T

http://identifiers.org/hco/1/GRCh38#94101452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121858284-C-A

94101751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121858016-C-T

94101865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121857980-G-C

94101872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121857978-A-G

94101973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121857878-G-A

94102301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121857552-T-C

http://identifiers.org/hco/1/GRCh38#94102562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121856755-C-A

94102562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121856755-C-T

94102805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121856526-C-T

94102806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121856525-C-T

94102966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121856380-G-A

94102966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121856380-G-C

94103009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121856352-C-T

94103016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 121856345-T-C

94103080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: stop gained
orthologous variants: 121856281-T-A

http://identifiers.org/hco/1/GRCh38#94103145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121856216-A-C

94103145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121856216-A-G

94103217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121856149-T-C

94103217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121856149-T-G

94103376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121855983-G-C

94103440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121855920-G-T

94103458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121855899-G-A

94103572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121855789-C-T

94103815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121854125-T-G

94103823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121854117-G-A

94103872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121854065-C-T

94103948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121853988-G-A

94103957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121853979-G-A

94104100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121853825-A-G

94104613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121853405-G-A

94104956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121853078-C-T

94104967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121853067-A-G

94105032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121853032-T-A

94105338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852707-G-A

94105465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852568-G-A

94105465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852568-G-T

http://identifiers.org/hco/1/GRCh38#94105499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121852531-A-C

http://identifiers.org/hco/1/GRCh38#94105534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121852495-A-C

94105566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852445-G-A

94105566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852445-G-C

94105781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852275-A-G

94105897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852164-C-T

94105898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852159-C-T

http://identifiers.org/hco/1/GRCh38#94105905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121852152-C-A

http://identifiers.org/hco/1/GRCh38#94105960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121852101-C-A

94106018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121852051-C-T

94106131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121851962-C-T

http://identifiers.org/hco/1/GRCh38#94106149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121851942-C-A

94106149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121851942-C-T

94106181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121851918-G-C

94106356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121851717-C-T

94107086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121850855-C-T

94107127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121850815-T-C

94107687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121849876-A-T

94107748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121849814-C-T

94107916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121849657-C-T

94108049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121849510-T-C

94108088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121849472-G-A

94108088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121849472-G-C

94108112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121849442-T-C

http://identifiers.org/hco/1/GRCh38#94108526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121849163-C-A

94108526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121849163-C-G

http://identifiers.org/hco/1/GRCh38#94108600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121849081-C-A

94108600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121849081-C-G

94108600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121849081-C-T

94108661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121849020-G-C

94109309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121848695-G-A

http://identifiers.org/hco/1/GRCh38#94109373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121848634-C-A

http://identifiers.org/hco/1/GRCh38#94109375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121848632-C-A

94109375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121848632-C-G

94109375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121848632-C-T

94109411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121848597-G-C

http://identifiers.org/hco/1/GRCh38#94110878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121848497-C-A

94111295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121848100-C-G

94111314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121848081-T-G

http://identifiers.org/hco/1/GRCh38#94111323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121848072-C-A

94111323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121848072-C-T

94111367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121848041-C-T

http://identifiers.org/hco/1/GRCh38#94111390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121848026-A-C

94112002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121847281-G-T

94112164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121847128-C-T

94112845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846744-A-G

94112845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846744-A-T

94112887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846705-C-T

94112896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846697-A-G

94112896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846697-A-T

94112919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846674-A-G

http://identifiers.org/hco/1/GRCh38#94112935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121846663-C-A

94112935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846663-C-T

94112938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846660-T-C

94112978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121846637-T-C

94112990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121846625-A-G

94113086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846530-A-G

94113134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846480-G-A

94113159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121846455-A-G

94113212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121845091-T-A

94113368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121844947-G-A

94113378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121844932-T-G

94113868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121844260-G-T

94113920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121844212-A-G

94113929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121844203-T-G

94113975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121844148-A-G

94114412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121843605-T-C

94114796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121843357-C-T

94114955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121843244-A-G

94115408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121842804-T-G

94115434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121842782-A-G

94115623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121842621-C-T

94115781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121842469-G-T

94116568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121842333-C-T

94116652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121842251-C-T

94116659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121842244-G-A

94117259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121841848-T-A

94117259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121841848-T-C

94117306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121841802-A-T

94117427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121841683-T-C

94117433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121841677-G-A

http://identifiers.org/hco/1/GRCh38#94117536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121841533-C-A

94117746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121841294-T-C

94117758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121841282-C-T

94118275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121840731-G-A

94118278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron_variant, undefined
orthologous variants: 121840728-G-A

94118436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121840613-G-C

94118624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121840444-G-A

94118763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121840333-G-A

94118848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121840267-A-T

94119004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121840180-A-G

94119023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121840163-T-C

94119042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121840139-C-T

94119184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121840000-C-T

94119482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121839695-C-T

94119531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121839640-G-C

94119915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121839210-T-A

94119946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121839165-C-T

94120247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121838845-G-T

94120683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121838486-G-A

94120710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121838464-G-C

http://identifiers.org/hco/1/GRCh38#94120771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121838399-A-C

94120771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121838399-A-T

94120772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121838398-C-T

http://identifiers.org/hco/1/GRCh38#94120883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121838319-C-A

94120883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121838319-C-G

94120883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121838319-C-T

http://identifiers.org/hco/1/GRCh38#94120884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121838318-C-A

94120884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: 121838318-C-T

http://identifiers.org/hco/1/GRCh38#94120928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121838276-C-A

94121026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: missense variant
orthologous variants: 121838213-A-G

94121068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 5 prime UTR variant
orthologous variants: 121838173-G-A

94121068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 5 prime UTR variant
orthologous variants: 121838173-G-C

94121070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 5 prime UTR variant
orthologous variants: 121838171-T-A

94121070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 5 prime UTR variant
orthologous variants: 121838171-T-C

94121116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34
most severe consequence: 5 prime UTR variant
orthologous variants: 121838123-T-C