128830446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 5 prime UTR variant
orthologous variants: 29433295-G-C

128830446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 5 prime UTR variant
orthologous variants: 29433295-G-T

128830611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 5 prime UTR variant
orthologous variants: 29433435-C-T

128830617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 5 prime UTR variant
orthologous variants: 29433439-G-A

128830928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous_variant, undefined
orthologous variants: 29433751-G-A

http://identifiers.org/hco/7/GRCh38#128831038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29433855-C-A

128831060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, undefined
orthologous variants: 29433873-G-A

128831060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, undefined
orthologous variants: 29433873-G-T

128831091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29433890-G-A

128831091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29433890-G-T

128831451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29434218-C-T

128831467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29434233-C-T

128831870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29434642-A-G

128832078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29434837-C-G

128832118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29434879-G-A

128832421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29435261-C-T

http://identifiers.org/hco/7/GRCh38#128832492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29435334-A-C

128832492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29435334-A-G

128832633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29435475-G-A

128833481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29436334-C-T

http://identifiers.org/hco/7/GRCh38#128833515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29436372-C-A

128833515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29436372-C-G

http://identifiers.org/hco/7/GRCh38#128833599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29436464-A-C

128833600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29436465-C-T

http://identifiers.org/hco/7/GRCh38#128833614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29436479-A-C

http://identifiers.org/hco/7/GRCh38#128833627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29436492-C-A

128833627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29436492-C-G

128833878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29436749-C-G

128834341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29437077-T-G

128834408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29437146-C-G

128834559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29437289-T-C

128834639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29437362-G-A

128834897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29437868-G-C

128834945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29437915-G-A

128835026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438064-A-T

128835045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438086-A-G

128835100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438179-C-T

128835112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438191-C-T

http://identifiers.org/hco/7/GRCh38#128835179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29438288-C-A

128835179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438288-C-T

128835229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438370-G-A

128835245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438392-A-G

128835298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438435-G-C

http://identifiers.org/hco/7/GRCh38#128835504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29438641-C-A

128835504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29438641-C-T

128835584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438721-C-T

http://identifiers.org/hco/7/GRCh38#128835634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29438772-C-A

128835634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438772-C-T

http://identifiers.org/hco/7/GRCh38#128835663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29438798-A-C

128835663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438798-A-G

http://identifiers.org/hco/7/GRCh38#128835695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29438831-C-A

128835695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438831-C-T

128835839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29438965-G-A

128836032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29439136-G-A

128836038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29439142-C-T

http://identifiers.org/hco/7/GRCh38#128836237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29439317-C-A

128836338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29439419-G-A

128836763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29439791-G-A

128836779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29439807-A-G

128837029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440047-G-C

128837033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440051-G-A

128837088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440107-G-A

128837088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440107-G-T

128837096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440115-A-T

128837124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440135-G-A

128837124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440135-G-T

http://identifiers.org/hco/7/GRCh38#128837139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29440150-C-A

128837139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440150-C-G

http://identifiers.org/hco/7/GRCh38#128837149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29440160-C-A

128837149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440160-C-T

http://identifiers.org/hco/7/GRCh38#128837293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29440304-A-C

128837293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440304-A-G

128837293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440304-A-T

128837297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440308-G-A

128837297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440308-G-C

128837297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440308-G-T

128837347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440358-G-A

http://identifiers.org/hco/7/GRCh38#128837496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29440494-C-A

128837496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29440494-C-T

http://identifiers.org/hco/7/GRCh38#128837535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29440533-C-A

128837535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29440533-C-T

128837544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29440542-G-A

128837547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 29440545-T-C

128837547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 29440545-T-G

128837576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440574-T-C

128837588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440591-C-T

128837608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440609-G-A

128837608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440609-G-C

128837707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29440707-G-T

128837737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29440737-T-C

http://identifiers.org/hco/7/GRCh38#128837749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29440749-C-A

128837749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29440749-C-T

128837752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29440752-G-A

128837752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense variant
orthologous variants: 29440752-G-T

128837769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440768-G-A

128837769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440768-G-T

http://identifiers.org/hco/7/GRCh38#128837969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29440857-C-A

128837969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29440857-C-T

128838022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29440911-C-G

128838296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29441127-T-A

128838739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29441569-C-T

128838884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29441746-G-A

128838884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29441746-G-C

http://identifiers.org/hco/7/GRCh38#128838926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29441784-C-A

128838926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29441784-C-G

128838926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29441784-C-T

128839070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29441924-C-G

128839070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29441924-C-T

128839206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442094-G-A

http://identifiers.org/hco/7/GRCh38#128839247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29442131-C-A

128839286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442169-G-A

128839293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442176-G-A

128839320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442205-G-A

128839762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442596-C-T

128839935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442779-G-A

128839935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442779-G-C

128839935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442779-G-T

128839971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442818-A-G

128839971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442818-A-T

128839998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442855-A-G

128840004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29442861-C-T

128840198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443042-G-A

128840238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443069-A-G

http://identifiers.org/hco/7/GRCh38#128840283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29443110-C-A

http://identifiers.org/hco/7/GRCh38#128840422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29443255-C-A

128840422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443255-C-T

128840690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443515-C-T

128841003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443837-T-C

128841003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443837-T-G

128841006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443840-G-A

128841006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443840-G-C

128841006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443840-G-T

128841122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443941-G-A

128841147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29443981-G-A

128841222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29444056-G-A

128841222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29444056-G-C

128841237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29444071-T-C

128841273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29444107-T-C

128841273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29444107-T-G

128841327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29444161-C-T

128841417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29444254-C-T

128841418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29444255-T-C

128841462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29444304-C-G

128841495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29444337-C-T

128841640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444448-G-T

128841803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444602-A-T

128842076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29444855-C-T

http://identifiers.org/hco/7/GRCh38#128842083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#29444862-C-A

128842083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29444862-C-T

128842101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29444869-T-C

http://identifiers.org/hco/7/GRCh38#128842130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29444895-A-C

128842130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444895-A-G

128842130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444895-A-T

http://identifiers.org/hco/7/GRCh38#128842189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29444952-C-A

128842189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444952-C-T

http://identifiers.org/hco/7/GRCh38#128842251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29445027-C-A

128842251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29445027-C-G

128842251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29445027-C-T

http://identifiers.org/hco/7/GRCh38#128842272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29445048-C-A

128842272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29445048-C-T

128842311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29445087-G-A

128842311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29445087-G-C

http://identifiers.org/hco/7/GRCh38#128842389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#29445165-C-A

128842389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29445165-C-T

128842390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29445166-C-T

128842521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445319-A-T

128842562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445362-A-G

128842562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445362-A-T

128843075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29445928-G-C

128843134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29445964-T-C

128843134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29445964-T-G

http://identifiers.org/hco/7/GRCh38#128843144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29445974-C-A

128843144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29445974-C-T

128843276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29446097-T-C

128843276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense variant
orthologous variants: 29446097-T-G

128843306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29446127-G-A

128843306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29446127-G-T

128843325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29446146-T-C

128843347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29446167-G-A

128843439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29446260-G-A

128843439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29446260-G-C

128843547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29446368-C-T

128843587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29446408-G-T

128843640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29446458-T-C

128843694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29446511-T-C

128843919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29446729-T-G

128843968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29446771-G-A

128843968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29446771-G-T

128844029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29446832-A-G

128844294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29447097-G-A

128844294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29447097-G-T

128844305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29447108-A-G

128844305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29447108-A-T

128844351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29447151-A-T

128844384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29447167-G-A

128844384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29447167-G-T

http://identifiers.org/hco/7/GRCh38#128844672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29447408-C-A

128844672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29447408-C-T

128844762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29447498-A-G

128844786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense variant
orthologous variants: 29447522-C-G

128844786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29447522-C-T

128845008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29447744-A-G

http://identifiers.org/hco/7/GRCh38#128845017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29447753-C-A

128845017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29447753-C-G

128845017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29447753-C-T

128845087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense variant
orthologous variants: 29447823-G-A

128845171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense variant
orthologous variants: 29447907-C-T

128845318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29448038-G-A

128845318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29448038-G-T

128845584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29448260-C-G

http://identifiers.org/hco/7/GRCh38#128845807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29448474-C-A

http://identifiers.org/hco/7/GRCh38#128845883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29448512-A-C

128845883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29448512-A-G

128845942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29448522-G-A

128846051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29448618-C-T

128846087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29448654-G-A

128846120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29448687-T-C

128846132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29448699-C-G

128846132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29448699-C-T

128846175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29448747-T-C

128846175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29448747-T-G

128846548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29449054-C-G

128846548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29449054-C-T

128846679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29449178-A-G

128846835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29449325-C-T

128846871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29449361-C-T

128846889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29449379-G-A

128846889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29449379-G-C

128846950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29449434-G-A

128847383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29450256-A-G

128847575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29450468-T-A

128847575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29450468-T-C

128847575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29450468-T-G

http://identifiers.org/hco/7/GRCh38#128847582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29450475-C-A

128847582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29450475-C-T

128848074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29450942-G-T

http://identifiers.org/hco/7/GRCh38#128848203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29451056-C-A

http://identifiers.org/hco/7/GRCh38#128848413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29451245-C-A

128848413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29451245-C-T

128848419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29451251-C-G

128848419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29451251-C-T

http://identifiers.org/hco/7/GRCh38#128848460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29451294-C-A

128848460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29451294-C-T

128848691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: missense variant
orthologous variants: 29451501-G-A

128848708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29451518-C-T

128849106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29451915-T-A

128849106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29451915-T-C

128849106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29451915-T-G

http://identifiers.org/hco/7/GRCh38#128849119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29451928-C-A

http://identifiers.org/hco/7/GRCh38#128849130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29451939-C-A

128849130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29451939-C-T

128849269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452070-C-T

128849270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452071-G-A

128849314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452115-G-C

128849314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452115-G-T

128849422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29452223-G-A

128849473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29452274-T-C

128849476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29452277-C-T

128849506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29452307-C-G

128849506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: synonymous variant
orthologous variants: 29452307-C-T

128849625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452422-C-T

http://identifiers.org/hco/7/GRCh38#128849844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29452685-C-A

128849844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452685-C-T

128849926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452751-T-A

128849926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452751-T-C

http://identifiers.org/hco/7/GRCh38#128850008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29452830-C-A

128850008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 29452830-C-T

128850015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant
orthologous variants: 29452837-G-A

128850015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant
orthologous variants: 29452837-G-T

http://identifiers.org/hco/7/GRCh38#128850027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29452849-C-A

128850027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant
orthologous variants: 29452849-C-T

128850080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron variant
orthologous variants: 29452903-G-A

http://identifiers.org/hco/7/GRCh38#128850231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29453052-C-A

128850231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29453052-C-T

http://identifiers.org/hco/7/GRCh38#128850254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29453075-C-A

128850254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29453075-C-T

128850464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29453278-G-A

128850511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453329-G-A

128850511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453329-G-C

128850511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453329-G-T

http://identifiers.org/hco/7/GRCh38#128850528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29453338-C-A

128850528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453338-C-G

128850528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453338-C-T

128850582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453398-G-C

128850582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453398-G-T

http://identifiers.org/hco/7/GRCh38#128850659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29453471-C-A

128850659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453471-C-G

http://identifiers.org/hco/7/GRCh38#128850670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29453482-C-A

128850670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453482-C-T

http://identifiers.org/hco/7/GRCh38#128850677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29453494-C-A

128850677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453494-C-T

128850810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29453626-G-A

128850810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29453626-G-C

128850840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29453656-C-T

128850882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29453698-T-C

128850882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 29453698-T-G

http://identifiers.org/hco/7/GRCh38#128850987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29453797-C-A

128851033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453843-T-C

http://identifiers.org/hco/7/GRCh38#128851062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29453872-C-A

128851062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453872-C-T

128851189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453998-A-G

128851275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29454085-T-A

128851275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29454085-T-C

128851375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454186-G-A

128851396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454202-C-T

http://identifiers.org/hco/7/GRCh38#128851522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29454328-C-A

128851522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29454328-C-G

128851522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29454328-C-T

128851649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454455-T-A

128851649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454455-T-C

http://identifiers.org/hco/7/GRCh38#128851739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29454513-C-A

128852263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454871-G-A

128852272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454889-G-A

128852574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455098-C-T

http://identifiers.org/hco/7/GRCh38#128852581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29455109-C-A

128852581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455109-C-G

128852581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455109-C-T

128852794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455324-A-G

http://identifiers.org/hco/7/GRCh38#128852795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29455325-C-A

128852795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455325-C-G

128852795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455325-C-T

http://identifiers.org/hco/7/GRCh38#128852853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29455385-C-A

128852853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29455385-C-G

128852853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29455385-C-T

http://identifiers.org/hco/7/GRCh38#128852862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29455394-C-A

128852862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29455394-C-T

128852931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29455463-T-C

128852931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29455463-T-G

128852979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29455511-C-T

128853027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29455559-T-C

128853027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29455559-T-G

128853055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455587-C-T

128853102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455633-G-A

128853157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455681-G-C

128853171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455693-G-A

128853171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455693-G-C

128853178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455700-T-C

128853178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455700-T-G

128853183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455705-G-A

128853184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455706-G-T

http://identifiers.org/hco/7/GRCh38#128853199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29455721-C-A

128853199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455721-C-T

128853241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455766-G-A

128853241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455766-G-T

128853566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29455880-C-T

http://identifiers.org/hco/7/GRCh38#128853663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29455974-C-A

128853861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456179-T-A

128853865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456183-G-A

128853865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456183-G-T

128853874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456191-G-A

128854095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456412-G-A

128854266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456589-G-A

128854266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456589-G-T

128854291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456620-G-T

128854325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456653-C-G

128854325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456653-C-T

128854332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456660-G-A

http://identifiers.org/hco/7/GRCh38#128854342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29456669-C-A

128854342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456669-C-T

128854417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29456740-G-T

http://identifiers.org/hco/7/GRCh38#128854549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29456872-C-A

128854549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456872-C-T

128854579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456902-C-G

128854579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456902-C-T

128854609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456932-G-A

128854609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456932-G-C

128854609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456932-G-T

128854639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456962-G-A

128854654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29456977-G-C

128854816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29457141-C-T

128855010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457300-T-C

128855011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457301-C-G

128855011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457301-C-T

http://identifiers.org/hco/7/GRCh38#128855016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29457306-C-A

128855016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457306-C-T

128855131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457375-A-G

http://identifiers.org/hco/7/GRCh38#128855154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29457398-C-A

128855154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457398-C-T

128855221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29457464-G-A

128855230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29457473-T-A

128855230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29457473-T-C

http://identifiers.org/hco/7/GRCh38#128855251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29457494-C-A

128855251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29457494-C-T

http://identifiers.org/hco/7/GRCh38#128855284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29457527-C-A

128855284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29457527-C-T

http://identifiers.org/hco/7/GRCh38#128855302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29457545-C-A

128855302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29457545-C-T

128855353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457579-T-C

128855354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457580-G-T

128855391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457617-G-T

128855400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457626-T-C

128855404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457630-G-T

128855419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29457641-G-A

http://identifiers.org/hco/7/GRCh38#128855444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29457672-A-C

128856241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458527-A-G

128856374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458640-G-A

128856374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458640-G-T

128856440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458699-G-A

128856440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458699-G-T

128856483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458741-C-T

128856490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458748-G-A

128856490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458748-G-T

128856523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29458781-G-A

128856523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29458781-G-T

128856532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29458790-G-C

128856688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29458945-T-C

128856818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29459081-C-T

http://identifiers.org/hco/7/GRCh38#128857167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29459416-C-A

128857347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29459597-G-C

128857357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29459607-G-T

http://identifiers.org/hco/7/GRCh38#128857362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29459612-A-C

128857362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29459612-A-G

http://identifiers.org/hco/7/GRCh38#128857404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29459647-C-A

128857404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29459647-C-T

128857483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29459720-G-A

http://identifiers.org/hco/7/GRCh38#128857725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29460422-C-A

128857800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460497-G-C

128857884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460576-A-G

128857884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460576-A-T

http://identifiers.org/hco/7/GRCh38#128857913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29460603-C-A

http://identifiers.org/hco/7/GRCh38#128857943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29460626-C-A

128857943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460626-C-T

http://identifiers.org/hco/7/GRCh38#128857989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29460675-C-A

128857989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460675-C-T

128857999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460685-A-G

128857999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460685-A-T

128858089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29460775-G-A

128858089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29460775-G-C

128858093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29460779-C-T

128858102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29460788-C-T

http://identifiers.org/hco/7/GRCh38#128858198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29460884-C-A

128858198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29460884-C-T

128858227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460913-G-A

128858227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460913-G-C

128858227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460913-G-T

128858282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460976-G-T

128858304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460992-G-T

128858358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29461043-C-T

http://identifiers.org/hco/7/GRCh38#128858367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29461052-C-A

128858481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29461166-C-T

128858490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29461175-C-T

128858534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461219-T-C

128858706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461381-G-A

128858706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461381-G-T

128858763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461433-G-T

http://identifiers.org/hco/7/GRCh38#128858772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29461442-C-A

128858772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461442-C-G

128858772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461442-C-T

http://identifiers.org/hco/7/GRCh38#128858774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29461444-C-A

128858774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461444-C-T

128858776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461445-G-T

128858875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461540-G-A

128858875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461540-G-T

128858882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461547-G-A

128858882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461547-G-T

http://identifiers.org/hco/7/GRCh38#128858912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29461578-C-A

128858912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461578-C-T

128858960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461610-G-A

128858960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461610-G-T

http://identifiers.org/hco/7/GRCh38#128858965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29461615-C-A

128858965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461615-C-T

128859043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461684-T-A

128859043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461684-T-C

128859043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461684-T-G

http://identifiers.org/hco/7/GRCh38#128859046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29461687-C-A

128859046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461687-C-G

128859046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461687-C-T

128859150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3756
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29461785-C-T