http://identifiers.org/hco/4/GRCh38#37244894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807353-C-A

37244894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807353-C-T

37244898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807357-G-A

37244898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807357-G-C

37244898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807357-G-T

http://identifiers.org/hco/4/GRCh38#37244945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807404-C-A

37244945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807404-C-T

http://identifiers.org/hco/4/GRCh38#37244964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807423-C-A

37244964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807423-C-T

http://identifiers.org/hco/4/GRCh38#37244967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807426-C-A

37244967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807426-C-T

http://identifiers.org/hco/4/GRCh38#37245017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807465-C-A

37245017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807465-C-T

37245041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807488-G-A

37245041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 5 prime UTR variant
orthologous variants: 63807488-G-T

http://identifiers.org/hco/4/GRCh38#37245122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807567-C-A

37245122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63807567-C-T

http://identifiers.org/hco/4/GRCh38#37245175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807620-C-A

37245175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous_variant, undefined
orthologous variants: 63807620-C-T

37245240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63807689-G-T

http://identifiers.org/hco/4/GRCh38#37245254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807703-C-A

37245254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63807703-C-T

http://identifiers.org/hco/4/GRCh38#37245303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807747-C-A

37245303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63807747-C-G

37245303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63807747-C-T

37245308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63807752-G-A

37245308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63807752-G-T

37245331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63807783-G-C

37245331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63807783-G-T

http://identifiers.org/hco/4/GRCh38#37245545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63807956-C-A

37245786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63808146-C-G

37246141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63808435-C-T

37246669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63808969-C-T

http://identifiers.org/hco/4/GRCh38#37246695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63808981-A-C

37246969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63809255-T-C

37247370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63809651-G-A

37247490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63809818-C-G

37247529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63809859-T-A

37247529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63809859-T-C

37248057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63810050-A-G

37248084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63810077-A-G

37248291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63810271-C-T

37248498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63810456-G-C

37248539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63810482-C-T

37248756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63810702-A-G

37248756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63810702-A-T

37248937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63810878-G-A

37249448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63811539-G-A

37249489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63811579-G-A

37249765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63811856-A-G

37249855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63811941-T-C

http://identifiers.org/hco/4/GRCh38#37249906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63811992-C-A

37249967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63812051-C-T

37250185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63812255-C-G

37250549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63812621-G-T

37251430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63812819-G-A

37251446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63812835-A-G

37251508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63812888-T-C

37251882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63813415-T-C

http://identifiers.org/hco/4/GRCh38#37252490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63813914-A-C

37253715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63814543-G-A

37254307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63821276-A-G

37254609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63821571-A-T

37254720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63821682-T-C

http://identifiers.org/hco/4/GRCh38#37255073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63822539-C-A

37255237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63822713-G-A

37255251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63822727-A-G

37255266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63822745-T-A

37255288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63822767-T-C

37255419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63822887-G-A

37255796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63823717-C-G

37255809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63823730-G-A

37256152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63824080-G-A

37256174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63824102-G-T

37256202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63824131-A-G

37256315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63824301-T-G

http://identifiers.org/hco/4/GRCh38#37256457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63824442-C-A

37256533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63824520-T-A

37257604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63829113-A-G

37257615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63829124-G-A

37257669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63829186-G-A

37257797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63829321-A-G

37257978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63829509-T-C

37258022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63829559-G-C

37259265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63831683-A-G

37259408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63831837-T-C

37259507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63831931-C-T

37259688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63832916-G-C

37259771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63833005-G-A

37259773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63833007-A-T

37259929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63833127-A-G

37259964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63833162-C-G

37260018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63833206-T-C

37260108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63833286-G-A

37260146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63833325-T-A

37260617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63833759-A-G

37261802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63835898-G-T

37261989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63836097-G-A

37262060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63836164-C-T

37262220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63836338-G-A

37263887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63837197-C-T

http://identifiers.org/hco/4/GRCh38#37263958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63837257-A-C

37264001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63837299-C-T

37264063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63837353-C-G

37264074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63837363-G-A

37264098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63837387-A-G

37264185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63837472-C-T

37264653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63837943-G-C

http://identifiers.org/hco/4/GRCh38#37264755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63838066-C-A

37264767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63838081-C-T

37265486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63839069-G-C

37265530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63839111-G-A

37265730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63839287-A-T

37265882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63839389-G-T

37265903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63839396-G-A

37265903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63839396-G-T

37266540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63844781-G-A

http://identifiers.org/hco/4/GRCh38#37266555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63844796-C-A

37266657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63844914-G-A

37266803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63845096-A-G

37266871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63845163-G-A

http://identifiers.org/hco/4/GRCh38#37267168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63845459-C-A

37267254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63845546-G-T

37267466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63845752-A-G

http://identifiers.org/hco/4/GRCh38#37267473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63845758-C-A

37267483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63845802-T-C

37267925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846078-G-C

http://identifiers.org/hco/4/GRCh38#37268061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63846204-A-C

37268061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846204-A-G

37268083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846227-C-G

37268389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846517-A-T

37268398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846526-T-C

37268413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846541-C-T

http://identifiers.org/hco/4/GRCh38#37268672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63846794-A-C

37268676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846798-C-G

37268676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846798-C-T

37268689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846811-A-G

37268690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63846812-T-C

37268801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63847967-C-G

37268801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63847967-C-T

37268914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848079-T-C

37268951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848116-C-T

37268996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848160-G-A

37269179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848338-T-A

37269288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848443-A-T

37269312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848467-G-A

http://identifiers.org/hco/4/GRCh38#37269317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63848471-A-C

37269496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848656-T-A

37269554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848716-C-T

37269667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848830-A-T

37269840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63848957-A-G

37269933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63849039-C-T

37270056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63849148-C-G

37270174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63849272-A-G

37279126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63850954-G-A

37279383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63851210-A-T

37279399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63851225-A-G

37279597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63852086-T-A

37279795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63852228-T-A

37281864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63853324-T-C

37281904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63853364-G-C

37282165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63853619-C-T

37282190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63853644-A-G

37282416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63853895-T-C

37282634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63854109-A-G

37282673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63854142-T-A

37282748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63854178-C-T

37282997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63854910-A-G

37283072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63854966-G-C

37283201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63855057-G-A

37284698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63855962-G-C

37285045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63856287-C-T

http://identifiers.org/hco/4/GRCh38#37285086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63856329-A-C

37285528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63856661-A-G

37285537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63856671-T-C

http://identifiers.org/hco/4/GRCh38#37285709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63856857-A-C

37285756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63856933-T-C

37285779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63856957-C-T

37286098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63858124-C-T

37286380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63858944-T-A

37286425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63858984-T-C

37286516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63859074-A-T

37286651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63859211-G-C

37286695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63859253-G-A

37286695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63859253-G-C

37288746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63859878-C-T

37288791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63859918-G-C

37288846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63859957-C-T

37288852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63859963-C-T

37288893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63860002-G-A

37289071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63860620-C-G

37289112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63860661-G-A

37289122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63860670-G-A

37289377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63862396-A-G

37289632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63862643-G-A

37289655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63862657-G-A

37289669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63862673-G-A

37289685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63862689-C-T

37289752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63862758-A-G

37289838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63862841-T-A

37290820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63866415-T-G

37290867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63866458-G-T

http://identifiers.org/hco/4/GRCh38#37290880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63866471-C-A

37291176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63867469-A-G

37291214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63867500-C-G

37291214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63867500-C-T

37291241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63867528-A-G

37291375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63867672-A-G

37291396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63867693-A-G

37291768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868077-A-G

37291828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868152-A-G

37291894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868261-G-A

37291955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868316-G-A

37291964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868328-C-G

37292047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868410-A-G

37292130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868494-G-T

37292160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868523-T-G

37292193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868550-T-A

37292312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868668-A-G

37292418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868753-A-G

37292425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63868760-G-A

http://identifiers.org/hco/4/GRCh38#37292460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63868798-C-A

37293158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63869590-T-A

37293483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63869922-T-G

37293485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63869925-T-G

37293638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870146-G-A

37293644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870152-T-C

37293926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870432-A-G

37293995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870480-G-T

37294022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870507-A-G

37294048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870535-G-A

37294088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870576-T-A

37294107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870594-G-A

37294143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870630-A-G

37294176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63870663-T-C

37317832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63876064-C-T

37320229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63876734-G-A

37320316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63876816-A-G

37320460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63876979-A-G

37320521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877035-T-A

37320544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877059-T-C

37320555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877070-T-A

37320659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877173-G-A

37320689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877199-C-T

37320690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877200-C-T

37320766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877275-A-G

37321466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877688-C-T

37321536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63877759-T-C

http://identifiers.org/hco/4/GRCh38#37321782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63877997-C-A

37321974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63878194-C-G

http://identifiers.org/hco/4/GRCh38#37322027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63878250-A-C

37322242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63878470-G-A

37322256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63878484-A-T

37322493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63878697-G-A

37322501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63878703-G-A

37324588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63881119-G-A

37324588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63881119-G-T

37324767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63881282-C-T

37325020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63881531-C-T

37325309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63881834-G-T

37325322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63881847-A-G

37325349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63881881-G-A

37325409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63881945-T-C

37325528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882111-C-T

http://identifiers.org/hco/4/GRCh38#37325787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63882363-C-A

37325787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882363-C-G

37325787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882363-C-T

37325816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882392-C-T

37325837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882413-T-C

37325837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882413-T-G

37325883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882450-G-A

37325883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882450-G-C

37325883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882450-G-T

http://identifiers.org/hco/4/GRCh38#37325910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63882477-C-A

37325910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882477-C-G

37325937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 63882502-T-C

37325940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63882505-G-A

37325940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63882505-G-T

http://identifiers.org/hco/4/GRCh38#37325983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63882548-C-A

37325983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63882548-C-G

37325983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63882548-C-T

http://identifiers.org/hco/4/GRCh38#37326050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63882612-C-A

37326122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882676-G-T

37326127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882682-G-A

37326127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882682-G-C

37326127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63882682-G-T

37326867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63885648-C-G

37326947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63885729-A-G

37327259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63886040-G-A

37327481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63886249-G-A

37327648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63886384-C-T

37327788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63886525-C-T

37327997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63886744-T-G

37328001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63886751-C-G

37337166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63889369-C-T

37337257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63889458-C-T

37337446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63889639-G-A

37337454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63889646-C-T

37337772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63889914-C-G

37337774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63889916-T-C

37337883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63890012-G-A

37337883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63890012-G-C

37337905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63890033-G-A

37337907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63890035-C-T

37337974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63890109-A-G

37338551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63891762-G-A

37338598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63891810-C-T

37338632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63891843-T-A

37339134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63893050-A-G

37339179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63893093-T-A

37340253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63893843-T-A

37343472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63895378-G-A

37343550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63895461-T-C

37343746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63896453-A-G

37344125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63896853-C-T

http://identifiers.org/hco/4/GRCh38#37344169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63896897-A-C

37344169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63896897-A-G

37344169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63896897-A-T

37344286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63897014-G-A

http://identifiers.org/hco/4/GRCh38#37344353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63897081-A-C

37344527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63897254-T-A

37344625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63897345-C-T

37344849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63897643-T-C

37345119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63897852-A-G

37345143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63897876-C-T

37345175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63897912-T-C

http://identifiers.org/hco/4/GRCh38#37345385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63898083-A-C

37345529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63898242-T-G

37345572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63898282-G-C

37355026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63900738-G-A

37355063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63900772-G-A

37355063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63900772-G-C

37355170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63900883-A-G

37355170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63900883-A-T

37355614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63901569-C-T

http://identifiers.org/hco/4/GRCh38#37355739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63901856-A-C

37355774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63901891-C-T

37355881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63901997-T-C

37355995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902113-A-G

37356148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902251-T-C

37356207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902308-T-C

37356207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902308-T-G

http://identifiers.org/hco/4/GRCh38#37356220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63902324-C-A

37356220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902324-C-T

http://identifiers.org/hco/4/GRCh38#37356251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63902386-C-A

37356251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902386-C-T

http://identifiers.org/hco/4/GRCh38#37356264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63902400-A-C

37356264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902400-A-G

http://identifiers.org/hco/4/GRCh38#37356338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63902474-C-A

37356338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902474-C-T

37356410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63902568-C-T

37356522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902678-A-G

37356536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902692-T-G

http://identifiers.org/hco/4/GRCh38#37356616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63902862-C-A

37356616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902862-C-T

37356619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902865-T-C

37356620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902866-C-G

37356620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902866-C-T

37356650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902900-G-A

37356650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902900-G-C

http://identifiers.org/hco/4/GRCh38#37356684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63902934-C-A

37356684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63902934-C-T

37356788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63903211-A-T

37357088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63903510-C-T

37357112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63903535-A-G

37357291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63903870-C-T

37357293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63903872-G-A

37357293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63903872-G-T

37357300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63903879-T-G

37357652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63904225-T-C

37357765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63904334-A-G

37357959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63904493-C-T

http://identifiers.org/hco/4/GRCh38#37358041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63904564-C-A

37358528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63905019-A-G

http://identifiers.org/hco/4/GRCh38#37358924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63905349-A-C

37358989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63905412-G-C

37359251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63905673-A-G

37359253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63905675-T-G

http://identifiers.org/hco/4/GRCh38#37359343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63905764-C-A

37359343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63905764-C-T

37359652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63906031-T-C

http://identifiers.org/hco/4/GRCh38#37359873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63906206-A-C

37359897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63906230-G-A

37359980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63906299-A-G

37360005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63906323-A-T

37360160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63906434-A-G

37368139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63912053-C-T

http://identifiers.org/hco/4/GRCh38#37368283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63912226-C-A

37368283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63912226-C-T

37368289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63912232-G-A

37368314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63912270-T-C

37368360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63912299-T-C

37368492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63912387-T-C

37368761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63912637-G-A

37369694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63914169-A-T

37369698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63914173-G-A

37369698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63914173-G-T

37370138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63915084-T-C

37370477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63915125-C-T

37371397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63915742-A-G

37371404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63915749-C-G

37371414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63915759-A-G

37371484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63915825-A-G

37371536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63915877-A-G

37371581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63915922-T-C

37371681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63916008-C-T

37371860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63916188-A-G

37371930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63916258-T-G

37372252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63916626-G-A

37372343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63916716-T-A

37372529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63916897-T-G

37374487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63917032-G-A

37374879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63917617-C-T

http://identifiers.org/hco/4/GRCh38#37374904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63917644-A-C

37383102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63919466-T-C

37383174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63919524-G-A

37383174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63919524-G-C

37383674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63919974-C-T

37383815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63920109-C-T

37384183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63920320-T-A

37384272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63920401-G-A

37384272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63920401-G-T

37384469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63920620-G-A

37384715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63920854-G-C

37384724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63920861-A-G

http://identifiers.org/hco/4/GRCh38#37384841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63920971-C-A

37384847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63920977-A-G

37384892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63921022-G-A

37384892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63921022-G-T

37384962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63921103-C-T

37384981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63921122-T-A

http://identifiers.org/hco/4/GRCh38#37385028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63921193-C-A

http://identifiers.org/hco/4/GRCh38#37385338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63921414-C-A

37385624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63921663-A-T

37385797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63921817-G-T

http://identifiers.org/hco/4/GRCh38#37385898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63922075-A-C

37386009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63922180-G-C

37386038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63922207-G-A

37386269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63922435-C-G

http://identifiers.org/hco/4/GRCh38#37386289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63922462-A-C

37386530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63922670-C-T

37386533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63922673-T-C

37386642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63922765-A-G

37386663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63922786-C-G

37386663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63922786-C-T

37389238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63923724-A-G

37389275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63923761-C-G

37389367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63923825-T-C

37389450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63923904-C-T

37389476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63923931-C-T

37389571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63924040-G-A

37389791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63924235-T-A

37390182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63924303-C-T

37390337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63924384-G-A

37390474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63924515-T-C

37390543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63924588-C-T

37390759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63924730-C-T

37392956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63926394-G-A

37392956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63926394-G-C

37392958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63926396-T-G

37393100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63926531-G-A

37393184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63926601-A-G

37393206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63926618-C-T

37393351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63926765-G-A

http://identifiers.org/hco/4/GRCh38#37393556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63926956-A-C

37393886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63927279-T-C

37393969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63927345-T-C

37394207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63927560-T-C

37394305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63927654-A-G

http://identifiers.org/hco/4/GRCh38#37395645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63927933-A-C

37395645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63927933-A-G

37395718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63927992-T-C

37396453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63928701-C-T

37396725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63928994-T-C

37396731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63929000-G-A

37397776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63930139-C-T

37397820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63930159-T-A

http://identifiers.org/hco/4/GRCh38#37397944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63930272-A-C

37397944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63930272-A-G

37398024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63930360-T-G

37398586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63930602-C-G

http://identifiers.org/hco/4/GRCh38#37398625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63930641-C-A

http://identifiers.org/hco/4/GRCh38#37398626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63930642-C-A

37398626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63930642-C-T

37398979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63930888-C-T

37399098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63930997-T-C

37399325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63931218-T-C

37399412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63931851-G-A

37399412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63931851-G-T

37399525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63931958-T-C

37399615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63932049-G-T

37399832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63932455-A-G

37399920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63932541-T-C

37400042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63932669-G-A

37400175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63932785-T-G

37400224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63932834-G-A

37400446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63933061-C-T

37400451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63933066-G-A

37400469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63933082-T-G

37400492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63933111-G-C

37405248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63934424-G-A

37405291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63934466-C-T

37405761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935516-G-A

37405778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935533-A-T

37405926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935675-C-G

37405926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935675-C-T

37405950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935699-C-G

37405950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935699-C-T

37406008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935754-C-T

http://identifiers.org/hco/4/GRCh38#37406041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63935784-A-C

37406069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935809-A-G

37406074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935813-G-A

http://identifiers.org/hco/4/GRCh38#37406164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63935907-C-A

37406164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63935907-C-T

http://identifiers.org/hco/4/GRCh38#37414513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63937579-A-C

37414513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63937579-A-G

37414530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63937596-G-A

http://identifiers.org/hco/4/GRCh38#37414591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63937644-A-C

37414661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63937713-T-C

37414902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63937946-T-C

37414939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63937978-G-A

37415732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63940074-T-A

37415734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63940076-C-G

37415931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63940279-A-T

37416099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63940436-A-G

37419625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63941584-T-A

37419633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63941592-A-G

37419633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63941592-A-T

37419634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63941593-C-T

37419784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63941771-C-T

37419993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63941987-C-T

37420239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63942273-T-C

http://identifiers.org/hco/4/GRCh38#37420440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63942453-C-A

37420459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63942470-G-A

http://identifiers.org/hco/4/GRCh38#37420768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63942691-A-C

37420844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63942759-T-A

37420844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63942759-T-C

37421230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63942991-C-T

37421291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63943039-G-A

37421394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63943127-T-C

37421396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63943129-A-G

http://identifiers.org/hco/4/GRCh38#37421404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63943137-A-C

37421630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63943369-A-T

37423290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63944942-A-T

37423300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63944949-A-T

37424535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945315-A-G

37424562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945332-T-G

http://identifiers.org/hco/4/GRCh38#37424721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63945489-C-A

37424721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945489-C-G

37424721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945489-C-T

http://identifiers.org/hco/4/GRCh38#37424732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63945500-A-C

37424732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945500-A-G

37424732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945500-A-T

http://identifiers.org/hco/4/GRCh38#37424835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63945564-A-C

37424835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945564-A-G

37424835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945564-A-T

http://identifiers.org/hco/4/GRCh38#37424911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63945647-C-A

37424968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945703-G-A

37425091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63945819-T-C

37425208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946181-C-T

37425209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946182-A-T

37425217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946190-C-T

37425319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946294-T-C

37425491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946455-A-G

37425505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946469-G-A

37425505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946469-G-C

37425821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946733-A-G

37425946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946841-C-T

37426002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63946892-T-C

37426358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63947222-C-T

37426652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63947515-G-C

37426652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63947515-G-T

37426710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63947570-T-A

37429944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63948197-C-G

37430060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63948337-T-C

37430164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63948430-G-T

37430207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63948472-C-T

37430236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63948497-T-A

37430397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63948643-G-C

37430462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63948708-A-G

37430559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63948774-T-G

37430754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63948969-G-A

37432717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950004-A-T

37432828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950095-T-C

37433176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950414-C-T

37433206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950443-G-A

37433206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950443-G-C

http://identifiers.org/hco/4/GRCh38#37433237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63950474-C-A

37433237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950474-C-T

37433292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950527-A-T

37433565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950819-A-G

37433608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63950859-C-G

37433726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951394-T-C

37433726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951394-T-G

37433747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951424-C-T

37433758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951432-G-A

37433837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951492-T-C

37433876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 63951532-A-G

37433876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 63951532-A-T

37433926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63951582-A-G

37433992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63951648-C-G

37433992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63951648-C-T

37434040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951696-A-G

http://identifiers.org/hco/4/GRCh38#37434060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63951716-A-C

37434075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951731-T-C

http://identifiers.org/hco/4/GRCh38#37434080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63951736-C-A

37434080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951736-C-T

http://identifiers.org/hco/4/GRCh38#37434098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63951755-C-A

37434125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951764-G-T

37434129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63951768-T-C

37435311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63953517-G-T

37435587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63953930-T-A

37438298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63956888-A-G

37438678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63957260-T-C

37438704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63957287-A-G

37438763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63957342-G-T

37438940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63957517-T-C

37439186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63957763-T-C

37439295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63957872-A-G

http://identifiers.org/hco/4/GRCh38#37439404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63958006-C-A

37439404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958006-C-T

37439657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958234-T-C

37439717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958294-G-A

37439825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958397-G-A

37439825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958397-G-T

37439865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958437-C-T

http://identifiers.org/hco/4/GRCh38#37439923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63958497-A-C

37440016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958581-G-A

37440021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958586-C-G

37440182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958732-G-T

37440321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63958872-C-T

37441231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63959561-T-C

37441452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63959732-G-A

37441516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63959789-C-T

37441566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63959840-G-A

37441765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63960011-T-C

37441765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63960011-T-G

37441781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63960027-A-G

37441834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron_variant, undefined
orthologous variants: 63960067-A-G

37442228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63960423-C-G

37442351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63960546-A-G

37442371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63960566-T-C

37442380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63960583-C-T

http://identifiers.org/hco/4/GRCh38#37442554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63960839-C-A

37442637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63960916-C-G

37442752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63961235-G-A

37442752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63961235-G-T

37442827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63961308-A-G

37442967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63961442-A-G

37443147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: intron variant
orthologous variants: 63961584-T-G

37443363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63961792-A-G

37443363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63961792-A-T

37443525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63961954-T-C

37443554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63961983-T-C

37443800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63962229-A-G

37443944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63962373-G-A

37443971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63962400-T-G

37444373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63962802-G-A

37444418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63962847-T-C

37444544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63962973-C-T

37444889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63963318-C-T

37445096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63963525-T-C

37445189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63963618-C-T

http://identifiers.org/hco/4/GRCh38#37445207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63963636-A-C

37445207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63963636-A-G

37445207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63963636-A-T

37445312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63963741-G-T

37445471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63963900-C-G

37445471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63963900-C-T

37445489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63963918-T-C

37445999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63964428-C-T

37446134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63964563-T-C

http://identifiers.org/hco/4/GRCh38#37446149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63964578-C-A

http://identifiers.org/hco/4/GRCh38#37446176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63964605-C-A

37446176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63964605-C-G

37446176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63964605-C-T

37446248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63964677-C-T

37446431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63964860-C-T

37446444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63964873-T-C

37446617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63965046-G-T

37446709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63965138-G-A

37446709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63965138-G-C

37446709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: missense variant
orthologous variants: 63965138-G-T

37446770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63965199-T-C

37446962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63965391-C-T

http://identifiers.org/hco/4/GRCh38#37447205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63965634-C-A

37447205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63965634-C-G

37447205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: synonymous variant
orthologous variants: 63965634-C-T

37447251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63965681-T-C

http://identifiers.org/hco/4/GRCh38#37447297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63965745-C-A

37447409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63965836-A-G

37447436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63965864-T-A

37447436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63965864-T-G

37447447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63965875-T-A

37447447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63965875-T-G

37447598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966032-G-T

37447627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966064-G-T

37447796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966222-G-A

37447796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966222-G-T

37447905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966325-G-A

37447920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966340-A-G

37448000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966427-G-T

37448058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966483-A-G

37448138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966561-G-T

37448240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966661-T-G

37448245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966666-G-T

37448279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966700-T-C

37448303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966724-A-G

37448314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63966735-G-A

37448600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63967000-T-C

http://identifiers.org/hco/4/GRCh38#37448725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63967124-A-C

37448767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63967167-T-C

37448767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63967167-T-G

37449025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29229
most severe consequence: 3 prime UTR variant
orthologous variants: 63967431-G-T