42380557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82879904-T-C

42380888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880271-C-T

http://identifiers.org/hco/22/GRCh38#42380981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82880363-C-A

42380981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880363-C-T

42381037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880423-G-T

42381052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880437-C-T

42381345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880586-G-A

42381345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880586-G-T

http://identifiers.org/hco/22/GRCh38#42381426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82880629-C-A

42381426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880629-C-G

42381426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880629-C-T

42381482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880686-G-T

http://identifiers.org/hco/22/GRCh38#42381491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82880694-C-A

42381529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880717-A-G

42381533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880721-G-T

42381593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880755-C-T

42381595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880757-G-A

42381595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880757-G-C

42381595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880757-G-T

http://identifiers.org/hco/22/GRCh38#42381648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82880782-C-A

42381648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82880782-C-T

http://identifiers.org/hco/22/GRCh38#42382315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82881383-C-A

http://identifiers.org/hco/22/GRCh38#42382468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82881522-C-A

42382468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881522-C-T

42382504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881539-T-C

42382686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881659-T-C

42382689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881660-A-G

42382689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881660-A-T

42382690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881661-G-A

42382690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881661-G-T

http://identifiers.org/hco/22/GRCh38#42382745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82881716-C-A

42382745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881716-C-T

http://identifiers.org/hco/22/GRCh38#42382751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82881722-C-A

42382767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881738-C-T

http://identifiers.org/hco/22/GRCh38#42382854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82881828-C-A

42382854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881828-C-T

42382859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881834-G-A

42382859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881834-G-T

42382893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881872-A-G

42382893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881872-A-T

42382925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881904-A-G

http://identifiers.org/hco/22/GRCh38#42382986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82881965-C-A

42382986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881965-C-T

http://identifiers.org/hco/22/GRCh38#42383003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82881982-C-A

42383003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881982-C-G

42383003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881982-C-T

42383006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881985-G-A

42383006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82881985-G-T

42383032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882013-G-A

42383032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882013-G-T

42383071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882079-G-A

42383071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882079-G-T

42383093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882101-G-T

42383173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882179-G-A

42383173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882179-G-T

42383207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882207-A-G

42383280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882260-T-C

http://identifiers.org/hco/22/GRCh38#42383285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82882265-C-A

http://identifiers.org/hco/22/GRCh38#42383301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82882274-C-A

42383301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882274-C-T

42383302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882275-A-G

http://identifiers.org/hco/22/GRCh38#42383310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82882283-C-A

42383310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882283-C-T

42383356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882303-T-A

http://identifiers.org/hco/22/GRCh38#42383405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82882349-C-A

42383405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882349-C-T

http://identifiers.org/hco/22/GRCh38#42383421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82882363-C-A

42383421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882363-C-T

42383452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882392-A-G

42383453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882393-G-A

42383453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882393-G-T

42383575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882509-T-C

42383576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882510-G-T

42383611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882542-G-A

42383618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882560-T-C

42383675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882600-G-A

42383675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882600-G-T

42383715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882643-T-A

42383715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882643-T-C

42383738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882656-G-T

42383856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882766-A-G

42383856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882766-A-T

42383875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882795-A-G

http://identifiers.org/hco/22/GRCh38#42383918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82882833-C-A

42383918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882833-C-T

42383994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882890-A-G

42384049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882939-G-T

42384087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882978-G-A

42384087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82882978-G-T

42384139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883046-G-C

42384145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883052-A-G

42384184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883094-G-A

42384184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883094-G-T

42384298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883188-G-A

42384298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883188-G-C

42384298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883188-G-T

42384465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883285-C-T

42384468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883288-T-C

42384473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883293-T-A

42384473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883293-T-C

http://identifiers.org/hco/22/GRCh38#42384485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82883305-C-A

42384485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883305-C-T

http://identifiers.org/hco/22/GRCh38#42384486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82883306-C-A

42384486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883306-C-T

http://identifiers.org/hco/22/GRCh38#42384520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82883330-A-C

42384520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883330-A-G

42384582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883392-G-C

42384582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883392-G-T

http://identifiers.org/hco/22/GRCh38#42384657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82883462-C-A

http://identifiers.org/hco/22/GRCh38#42384668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82883473-C-A

42384668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883473-C-T

42384669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883474-T-G

42384709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883493-C-T

42384775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883549-G-T

42384939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883722-G-A

42384980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883761-G-A

42384980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883761-G-T

http://identifiers.org/hco/22/GRCh38#42385061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82883840-C-A

42385061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883840-C-T

42385141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883920-T-C

42385158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 3 prime UTR variant
orthologous variants: 82883934-A-G

42385257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82884030-A-G

http://identifiers.org/hco/22/GRCh38#42385306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82884234-C-A

42385440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82884361-C-T

42385651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82884673-A-G

42385665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82884687-C-T

42385951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885003-C-G

42385962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885013-C-T

42386023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885061-G-A

42386480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885152-C-G

42386618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885259-C-T

42386754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885389-G-A

42386838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885467-T-C

42386869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885496-A-G

42386869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885496-A-T

http://identifiers.org/hco/22/GRCh38#42386881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82885505-C-A

42386881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885505-C-T

42386924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885550-T-C

http://identifiers.org/hco/22/GRCh38#42386928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82885554-C-A

42386928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885554-C-T

42386948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885574-T-C

42386948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885574-T-G

42387047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 82885671-G-A

42387047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense variant
orthologous variants: 82885671-G-C

42387047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense_variant, stop_gained
orthologous variants: 82885671-G-T

42387049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 82885673-A-G

42387069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense variant
orthologous variants: 82885693-G-A

42387069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense variant
orthologous variants: 82885693-G-T

42387081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 82885705-A-G

42387094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885718-T-A

42387094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885718-T-C

42387097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885721-C-T

42387101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885725-A-G

42387113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885737-T-A

42387113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885737-T-C

http://identifiers.org/hco/22/GRCh38#42387129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82885753-C-A

42387129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885753-C-G

42387129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885753-C-T

http://identifiers.org/hco/22/GRCh38#42387208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82885878-C-A

42387212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885882-G-A

42387212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885882-G-T

42387335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82885978-C-G

42387387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886023-G-A

42387531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886153-T-A

42387531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886153-T-C

42387531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886153-T-G

http://identifiers.org/hco/22/GRCh38#42387741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82886351-C-A

http://identifiers.org/hco/22/GRCh38#42387802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82886399-C-A

http://identifiers.org/hco/22/GRCh38#42387971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82886512-C-A

42387971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886512-C-T

42388196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886718-G-A

42388221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886743-C-G

http://identifiers.org/hco/22/GRCh38#42388251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82886773-C-A

42388392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886917-A-T

42388394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886919-A-G

42388427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82886944-G-C

42388561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887066-G-A

42388733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887235-C-G

42388733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887235-C-T

42388793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887292-G-A

42388949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887389-G-A

42389225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887558-T-C

42389235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887573-G-C

42389258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887596-T-A

42389258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887596-T-G

42389683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887888-C-T

42389735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82887930-G-A

42389818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82888004-C-T

42389959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82888142-G-A

42390934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82888938-G-A

42396846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82893579-G-A

42397007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82893643-C-G

42397007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82893643-C-T

42397030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82893662-C-T

http://identifiers.org/hco/22/GRCh38#42397066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82893675-C-A

42397563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894092-T-A

42397738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894497-A-G

42397744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894503-G-A

42397744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894503-G-T

42397745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894504-G-T

42397750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894509-G-A

42397750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894509-G-T

42397757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894516-C-T

42397810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894536-G-T

42397835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894561-G-C

42397835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894561-G-T

42397844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894562-G-A

42397844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894562-G-C

42397844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894562-G-T

http://identifiers.org/hco/22/GRCh38#42397867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82894585-A-C

42397867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 82894585-A-G

42397867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 82894585-A-T

42397894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: stop_gained, synonymous_variant
orthologous variants: 82894612-G-A

42397923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense variant
orthologous variants: 82894641-T-C

42397943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 82894661-C-T

http://identifiers.org/hco/22/GRCh38#42397998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82894726-C-A

42397998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894726-C-G

42397998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894726-C-T

42398076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894806-T-C

http://identifiers.org/hco/22/GRCh38#42398082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82894812-C-A

42398102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894832-A-G

42398107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82894837-G-T

42399636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82895472-C-T

42399664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82895509-C-T

42399863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82895678-G-A

http://identifiers.org/hco/22/GRCh38#42400989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82896420-C-A

42401331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82896634-G-A

42401375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82896691-C-T

42401414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82896749-G-A

42401536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82896867-G-A

42401536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82896867-G-C

http://identifiers.org/hco/22/GRCh38#42401579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82896910-A-C

42401579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82896910-A-T

42401931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82897272-G-C

42401972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82897313-T-G

42402438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82897736-T-G

42402474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82897776-C-G

42402474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82897776-C-T

42408745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82898401-G-A

http://identifiers.org/hco/22/GRCh38#42409253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82898990-C-A

42409554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 82899235-G-A

42409554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 82899235-G-T

42409944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82899600-G-T

42410132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82899759-C-G

42410174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82899799-A-G

42410252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82899874-A-G

42410265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82899887-G-T

42410281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82899905-A-G

42410292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82899916-G-C

42410292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82899916-G-T

42410918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82900397-G-A

42410918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82900397-G-T

42410979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82900467-C-G

42410988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82900476-A-T

http://identifiers.org/hco/22/GRCh38#42411401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82900539-C-A

42411401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82900539-C-G

42411401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82900539-C-T

42411555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82900684-A-G

42411630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82900761-C-G

42411630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82900761-C-T

42411728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82900857-A-T

42411784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82900924-T-C

42411791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82900930-C-T

http://identifiers.org/hco/22/GRCh38#42412482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82901065-C-A

42412482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82901065-C-T

42412499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82901083-G-C

42412568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82901155-C-T

42412646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82901218-C-T

42412760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82901322-G-A

42412763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82901325-G-C

42412908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82901461-C-T

42413069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82901609-A-G

42413152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82901691-C-T

42413344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82901869-G-C

42415061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82903451-G-C

42415745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82903730-C-G

42415861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82903854-C-T

42415880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82903874-G-A

42415906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82903893-C-G

42415906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82903893-C-T

http://identifiers.org/hco/22/GRCh38#42417060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82905532-C-A

42417060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82905532-C-G

42417060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82905532-C-T

42417125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82905597-G-A

42417506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82905933-G-C

42417628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82906014-T-A

42417628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82906014-T-G

42418982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82907747-C-T

42419086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82907831-C-T

42419112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82907858-T-C

42419497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908130-G-A

42419502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908136-C-G

42419502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908136-C-T

42420013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908180-T-C

42420013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908180-T-G

42420028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908209-T-A

42420028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908209-T-G

42420159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908328-C-T

42420627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908750-A-G

42420630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908753-G-A

42420634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908757-C-T

42420637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908760-G-A

42420638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908761-C-T

42420658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908780-C-T

42420681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908803-G-A

42420681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908803-G-C

http://identifiers.org/hco/22/GRCh38#42420711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82908821-A-C

42420798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82908924-G-A

42420914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909047-G-A

42420914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909047-G-T

42420916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909049-T-C

42421842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909595-C-T

42421970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909725-T-A

42422077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909818-C-T

42422172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909926-G-A

42422189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909944-C-T

42422193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82909948-G-C

42424665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82910585-G-A

42424710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82910632-T-A

42424817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82910776-G-T

42426347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82911827-T-A

42426675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82912143-G-A

42426675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82912143-G-T

42426705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82912172-C-G

42426729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82912196-G-A

http://identifiers.org/hco/22/GRCh38#42426730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82912197-C-A

42426912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82912325-G-A

42427084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82912477-T-C

42427085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82912478-T-C

42427085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82912478-T-G

http://identifiers.org/hco/22/GRCh38#42427095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82912488-A-C

http://identifiers.org/hco/22/GRCh38#42427610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82913427-C-A

42428040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82914028-C-T

http://identifiers.org/hco/22/GRCh38#42428134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82914122-C-A

42428298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82914367-C-T

42428374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82914447-C-T

42428680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82914647-C-T

http://identifiers.org/hco/22/GRCh38#42431408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82916545-C-A

42431434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916568-G-A

42431465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916600-G-A

42431507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916643-C-T

42431580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916707-T-C

42431582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916709-G-T

42431656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916786-C-T

42431704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916832-G-T

42431797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916889-G-A

42431797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916889-G-C

42431799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916891-T-A

42431799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916891-T-C

42431799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916891-T-G

42431839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916928-C-T

http://identifiers.org/hco/22/GRCh38#42431902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82916978-A-C

42431903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82916979-G-C

42432075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82917161-C-G

42432197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82917280-G-A

42432197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82917280-G-T

42432319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82917390-G-C

42432319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82917390-G-T

http://identifiers.org/hco/22/GRCh38#42432335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82917409-C-A

42432335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 82917409-C-T

42432371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82917469-T-C

42432384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82917482-T-C

42432388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82917486-T-A

42432388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82917486-T-C

42432487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82917619-C-T

42432499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82917631-A-G

42432572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82917706-G-A

http://identifiers.org/hco/22/GRCh38#42432695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82917781-A-C

42432799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82917870-T-C

42432851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82917916-G-A

42432938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918036-A-T

42432997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918094-C-G

42433128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918269-C-T

42433154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918301-G-T

42433183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918335-C-G

42433197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918349-C-T

42433378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918483-G-A

42433380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918485-T-A

42433407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918511-C-T

42433415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918519-C-T

42433432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918536-T-C

42433546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918669-G-A

42433612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918735-A-G

http://identifiers.org/hco/22/GRCh38#42433626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82918749-C-A

42433729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918857-C-T

42433731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82918858-C-T

42434851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82919838-G-A

42434853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29872
most severe consequence: intron variant
orthologous variants: 82919840-C-T