42081994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93137757-T-C

42082117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93137882-A-G

42082291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138027-G-A

42082291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138027-G-C

42082350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138086-G-T

http://identifiers.org/hco/12/GRCh38#42082778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93138263-C-A

42083039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138529-T-C

42083045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138535-G-T

http://identifiers.org/hco/12/GRCh38#42083080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93138566-C-A

42083080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138566-C-G

42083103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138589-T-A

42083110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138596-G-T

http://identifiers.org/hco/12/GRCh38#42083114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93138600-C-A

42083114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138600-C-G

42083114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138600-C-T

42083143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138630-G-C

42083143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138630-G-T

42083146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138633-T-A

http://identifiers.org/hco/12/GRCh38#42083288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93138942-A-C

42083288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138942-A-T

42083318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93138969-G-A

http://identifiers.org/hco/12/GRCh38#42083574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93139236-C-A

42083655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93139499-G-T

42083945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93139825-T-C

42084255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140038-T-C

42084255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140038-T-G

42084256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140039-G-A

42084256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140039-G-C

42084256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140039-G-T

42084266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140045-T-C

42084370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140124-A-G

42084404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140165-A-G

http://identifiers.org/hco/12/GRCh38#42084452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93140204-C-A

42084452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140204-C-T

42084518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140252-A-G

42084607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140325-A-G

42084608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140326-A-G

42084608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140326-A-T

42085548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140657-T-A

42085548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140657-T-C

42085581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140690-A-G

42085776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 93140849-A-G

42085785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 93140858-A-G

42085827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 93140912-C-T

http://identifiers.org/hco/12/GRCh38#42085906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93140983-C-A

42085906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93140983-C-T

42085970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141139-A-G

http://identifiers.org/hco/12/GRCh38#42086198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93141294-C-A

http://identifiers.org/hco/12/GRCh38#42086204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93141300-C-A

42086204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141300-C-T

http://identifiers.org/hco/12/GRCh38#42086222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93141318-C-A

42086397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141488-G-A

42086397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141488-G-T

42086483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141549-A-G

42086547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141633-G-C

42086557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141643-T-C

42086576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141662-A-G

http://identifiers.org/hco/12/GRCh38#42086872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93141922-C-A

42086872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93141922-C-T

42087301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142394-G-A

42087418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142499-T-C

42087494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142575-T-C

42087494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142575-T-G

http://identifiers.org/hco/12/GRCh38#42087566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93142642-C-A

42087600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142676-G-A

42087600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142676-G-T

http://identifiers.org/hco/12/GRCh38#42087620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93142696-C-A

42087620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142696-C-T

42087624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142700-T-C

42087700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142769-T-C

42087720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142787-A-G

42087745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142808-A-G

42087745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 3 prime UTR variant
orthologous variants: 93142808-A-T

42087814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93142877-C-T

42087841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93142904-T-C

42087864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93142927-T-C

42087891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93142954-T-A

42087891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93142954-T-C

42087900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93142963-T-C

42087912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93142975-T-C

42087981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93143025-T-A

http://identifiers.org/hco/12/GRCh38#42088004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93143044-A-C

42088004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93143044-A-G

42088004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93143044-A-T

42088006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93143046-T-C

42088155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93143194-G-A

42088158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93143197-G-A

42088237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93143451-T-A

42088510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93144060-G-A

42088510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93144060-G-C

http://identifiers.org/hco/12/GRCh38#42097223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93145580-C-A

42097381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93145689-A-G

42097425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93145723-G-A

42097425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93145723-G-C

42097493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93145791-G-A

42097647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93145956-A-T

42097894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93146224-G-T

42097929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93146259-G-A

42097929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93146259-G-C

42097929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93146259-G-T

42098007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93146337-T-C

http://identifiers.org/hco/12/GRCh38#42098014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93146344-C-A

42098014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93146344-C-T

42098015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: stop gained
orthologous variants: 93146345-G-A

42098091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93146414-A-G

http://identifiers.org/hco/12/GRCh38#42098095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93146418-C-A

42098095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93146418-C-G

42098095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93146418-C-T

42098124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93146445-T-C

http://identifiers.org/hco/12/GRCh38#42098131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93146452-C-A

42098139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93146459-A-G

42098139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93146459-A-T

42098158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93146482-A-G

http://identifiers.org/hco/12/GRCh38#42098184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93146507-A-C

http://identifiers.org/hco/12/GRCh38#42103317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93149249-C-A

42103317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93149249-C-T

42103341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93149270-C-G

42103641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93149557-T-C

42104116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93149661-A-T

42104276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93149812-T-A

42104311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93149847-G-A

42104311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93149847-G-T

http://identifiers.org/hco/12/GRCh38#42104381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93149910-C-A

42104388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93149917-T-C

42105723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152099-A-T

42105737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152113-T-C

42105737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152113-T-G

42105784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152139-G-T

42105799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152160-A-G

http://identifiers.org/hco/12/GRCh38#42105830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93152194-C-A

42106007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93152371-T-A

42106007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93152371-T-C

42106007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93152371-T-G

42106034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93152398-G-A

42106034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93152398-G-C

42106034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93152398-G-T

42106046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93152410-T-A

42106046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93152410-T-G

42106113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152473-A-T

42106356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152670-T-C

42106389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152703-G-C

42106468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152770-T-C

42106574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93152847-T-C

http://identifiers.org/hco/12/GRCh38#42108144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93154729-C-A

42108184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93154766-G-A

42108200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93154781-C-T

42108373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93154909-A-T

42108408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93154944-T-A

42109523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93156902-T-A

42109539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93156918-A-G

42109540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93156919-A-G

42109540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93156919-A-T

42109618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93156998-G-A

42109619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93156999-C-T

http://identifiers.org/hco/12/GRCh38#42109629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93157009-A-C

42109629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93157009-A-G

42109671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93157051-T-A

42109671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93157051-T-C

http://identifiers.org/hco/12/GRCh38#42109698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93157078-C-A

42109698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 93157078-C-T

42109776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93157173-A-G

42109793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93157190-A-G

42109808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93157205-T-A

42109808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93157205-T-G

42109821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93157209-G-A

http://identifiers.org/hco/12/GRCh38#42110062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93157613-C-A

42110810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93158528-T-C

42110839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93158561-G-A

42118955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93159584-T-C

42119017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93159645-G-C

42119024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93159652-C-G

42119048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93159676-T-C

42120231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93160182-T-C

42120334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93160285-C-T

42120366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93160306-G-C

42121886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93161675-T-C

42121937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93161725-G-A

42121964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93161752-A-G

42121974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93161762-G-A

42122253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93162005-A-T

42129648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93163637-A-G

42129667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93163666-A-G

42129695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93163688-G-C

42129695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93163688-G-T

42129798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 93163791-T-C

http://identifiers.org/hco/12/GRCh38#42129866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93163855-C-A

42129866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93163855-C-G

42129866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93163855-C-T

42129891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93163879-T-C

42130142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93164120-A-G

42130306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93164266-T-A

42131222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron_variant, undefined
orthologous variants: 93164482-G-A

42131365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93164619-G-C

42131603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93164875-G-A

42131812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93165038-T-G

http://identifiers.org/hco/12/GRCh38#42132108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93165337-A-C

42138696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93169525-A-G

42139032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93169896-T-C

http://identifiers.org/hco/12/GRCh38#42139118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93169982-C-A

42139455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170299-C-G

42139465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170309-G-A

42139479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170323-C-G

42139513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170343-T-C

42139617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170417-G-C

42139710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170498-G-A

42139726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170510-T-C

42139732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170515-C-T

42139775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93170564-G-A

42143723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93172222-G-C

42143868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93172382-G-A

42144136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: intron variant
orthologous variants: 93172607-C-T

42144441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93172772-G-A

42144441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93172772-G-C

42144441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93172772-G-T

42144479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93172798-G-A

42144479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93172798-G-C

42144479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93172798-G-T

http://identifiers.org/hco/12/GRCh38#42144484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93172803-C-A

42144484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93172803-C-G

42144484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93172803-C-T

42144599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: synonymous variant
orthologous variants: 93172915-G-A

42144599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93172915-G-C

42144599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: missense variant
orthologous variants: 93172915-G-T

http://identifiers.org/hco/12/GRCh38#42144672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93173014-C-A

42144672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173014-C-G

42144672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173014-C-T

42144673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173015-G-A

42144673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173015-G-C

42144673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173015-G-T

http://identifiers.org/hco/12/GRCh38#42144677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93173019-C-A

42144677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173019-C-G

42144677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173019-C-T

http://identifiers.org/hco/12/GRCh38#42144681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93173023-C-A

42144681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173023-C-T

http://identifiers.org/hco/12/GRCh38#42144691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93173033-C-A

42144691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173033-C-G

42144691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173033-C-T

http://identifiers.org/hco/12/GRCh38#42144801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93173129-C-A

42144801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173129-C-T

http://identifiers.org/hco/12/GRCh38#42144817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93173145-C-A

42144817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173145-C-T

http://identifiers.org/hco/12/GRCh38#42144831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93173159-C-A

42144831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173159-C-G

42144831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173159-C-T

http://identifiers.org/hco/12/GRCh38#42144846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#93173172-A-C

42144846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27482
most severe consequence: 5 prime UTR variant
orthologous variants: 93173172-A-G