37365592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94369600-T-G

37365732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 94369760-T-C

37365769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 94369800-A-G

http://identifiers.org/hco/21/GRCh38#37366134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#94370004-C-A

37366134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94370004-C-G

37366193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94370034-C-G

37366222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94370057-T-G

http://identifiers.org/hco/21/GRCh38#37366391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#94370157-C-A

37366454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94370239-G-A

37366473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94370257-C-T

37366636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94370400-G-A

37367378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94371139-G-A

37367678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371441-C-G

37367678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371441-C-T

37367712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371473-G-A

37367844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371580-T-C

37367844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371580-T-G

http://identifiers.org/hco/21/GRCh38#37367920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94371630-C-A

37367920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371630-C-G

37367920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371630-C-T

http://identifiers.org/hco/21/GRCh38#37368112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94371817-C-A

37368112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94371817-C-T

37368137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371840-G-T

http://identifiers.org/hco/21/GRCh38#37368188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94371891-C-A

37368188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371891-C-T

37368215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371918-C-T

37368289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94371977-G-A

37368352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372039-C-G

37368352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372039-C-T

37368493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372176-C-G

37368631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372304-T-C

37368657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372319-C-T

37368658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372320-G-T

37368962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372584-G-A

37368965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372587-C-T

37368978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372600-A-G

37369001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372619-G-A

37369011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372629-A-G

37369190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372787-A-G

37369427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94372981-A-G

37369695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94373203-A-T

37371167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94374475-G-A

37376818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94377763-A-G

37376908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94377843-C-T

37378653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94379803-A-G

37378693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94379845-T-A

37378693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94379845-T-C

37378961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94380035-A-G

37378991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94380055-G-A

37379053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94380100-A-G

37379270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94380228-A-G

http://identifiers.org/hco/21/GRCh38#37379562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94380477-A-C

37379621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94380535-A-T

37379643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94380557-A-G

37379977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94381302-A-T

37380012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94381335-A-G

37380469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94381750-T-C

37380474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94381755-A-G

http://identifiers.org/hco/21/GRCh38#37380555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94381830-C-A

37380555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94381830-C-G

37380844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94382558-C-T

37381440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94383197-G-A

37382286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94384187-G-C

37382344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94384240-C-T

37391922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94386900-C-T

http://identifiers.org/hco/21/GRCh38#37391939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94386919-C-A

37391939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94386919-C-T

37391942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94386922-G-A

37392182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94387152-G-A

http://identifiers.org/hco/21/GRCh38#37392474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94387424-A-C

37392474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94387424-A-G

37393483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94388080-G-A

37397388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94390508-C-T

37399391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94391937-C-T

37399676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94392130-A-G

37399785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94392215-T-G

37399819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94392230-G-C

37400066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94392476-G-A

37400066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94392476-G-T

37400161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94392566-A-G

37400654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94392993-T-C

37405225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94398065-C-T

37405394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94398173-G-A

http://identifiers.org/hco/21/GRCh38#37405415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94398192-C-A

37405429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94398206-C-G

37405445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94398222-C-T

37405684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94398425-A-G

37405693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94398436-G-A

37405705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94398448-T-C

37407980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94400157-A-G

37408028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94400201-C-G

37408054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94400224-T-A

37408148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94400307-C-T

37408257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94400414-G-T

37408592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94400752-G-A

37408592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94400752-G-T

37408846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94400951-T-C

http://identifiers.org/hco/21/GRCh38#37410333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94402446-A-C

37410434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94402548-A-G

37413447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94404887-A-G

37413473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94404913-C-G

37413512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94404948-C-G

37413590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94405029-A-T

37413592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94405031-T-G

37413643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94405079-T-C

37413643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94405079-T-G

37413811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94405223-C-G

37413830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94405242-C-T

37413991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94405402-G-C

37414241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94406191-C-T

37415929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94406932-T-G

37416192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94407316-A-G

37416395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94407489-A-T

37417392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94408454-C-T

37417444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94408498-T-C

http://identifiers.org/hco/21/GRCh38#37417576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94408564-C-A

37417576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94408564-C-G

37417576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94408564-C-T

37417714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94408630-T-C

37417891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94408807-A-G

37418573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94410085-A-G

37418676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94410172-T-A

37418702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94410208-C-G

37418702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94410208-C-T

37419275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94410739-G-C

37419275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94410739-G-T

37419331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94410786-G-A

37419331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94410786-G-T

37419357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94410812-T-C

http://identifiers.org/hco/21/GRCh38#37419370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94410825-C-A

37419370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94410825-C-T

37419382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94410837-G-A

37419382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94410837-G-T

37419692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94411702-T-C

37419692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94411702-T-G

http://identifiers.org/hco/21/GRCh38#37419776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94411768-C-A

37420094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94412080-A-G

37420094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94412080-A-T

37420204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94412182-T-G

http://identifiers.org/hco/21/GRCh38#37420289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94412268-C-A

37420289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94412268-C-G

37420289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94412268-C-T

http://identifiers.org/hco/21/GRCh38#37420313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94412292-C-A

37420313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94412292-C-T

37420718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94412679-A-G

37420843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94412804-T-C

37420966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94412911-T-C

37421024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94412969-T-C

37421285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94413197-A-G

37421547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94413380-A-G

37421661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94413494-A-G

http://identifiers.org/hco/21/GRCh38#37421817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94413634-C-A

37421817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94413634-C-T

37422231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94414022-T-C

37422231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94414022-T-G

37422688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94414346-A-G

37422813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94414486-G-A

37422986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94414655-G-A

37423418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94415281-G-A

37424527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94416387-A-G

37428415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94423811-C-T

37429918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94427329-A-G

http://identifiers.org/hco/21/GRCh38#37430227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94427601-C-A

37430227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94427601-C-T

37430254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94427629-T-G

37430503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94427929-T-A

37430503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94427929-T-C

37430702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94428108-T-A

37430702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94428108-T-C

37430803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94428201-C-G

37431106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94428504-T-C

37431332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94428699-A-G

http://identifiers.org/hco/21/GRCh38#37431359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94428723-C-A

http://identifiers.org/hco/21/GRCh38#37431418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94428782-C-A

37431418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94428782-C-T

37431694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94429016-T-A

37431715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94429037-C-T

37432125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94429428-A-G

37432389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94429593-T-A

37432389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94429593-T-G

37432408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94429612-T-A

37432408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94429612-T-C

37432414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94429618-T-C

37433244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94430301-C-T

37433291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94430348-G-A

37433545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94430590-C-T

http://identifiers.org/hco/21/GRCh38#37433582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94430627-C-A

37433699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94431254-G-A

37434287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94432034-A-T

37434586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94432295-C-T

37435102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94432795-G-A

37435102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94432795-G-T

37435329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94433022-G-A

37435329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94433022-G-T

http://identifiers.org/hco/21/GRCh38#37435415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94433104-A-C

37435452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94433141-G-A

http://identifiers.org/hco/21/GRCh38#37436126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94434451-C-A

37436126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94434451-C-G

37436307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94434617-G-A

37436406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94434719-T-C

37436440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94434752-G-A

37436532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94434851-T-G

37436820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94435135-C-T

37436886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94435197-A-G

37436918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94435216-T-A

http://identifiers.org/hco/21/GRCh38#37437807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94435930-A-C

37437807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94435930-A-G

http://identifiers.org/hco/21/GRCh38#37437936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94436031-A-C

37437937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94436032-A-G

37437948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94436043-C-T

37438230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94436338-A-G

37438354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94436450-C-T

37438483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94436555-G-A

http://identifiers.org/hco/21/GRCh38#37438529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94436596-C-A

37448549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94446736-G-A

37448653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94446839-C-T

37451888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94449509-T-G

37451921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94449532-G-A

37452082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94449664-G-A

37452280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94449825-C-T

37452313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94449851-C-G

37452313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94449851-C-T

37452697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94450238-G-T

37453310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94450603-C-T

37453346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94450633-C-T

37453707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94451086-T-A

37453707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94451086-T-C

http://identifiers.org/hco/21/GRCh38#37455903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94452471-A-C

37455903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94452471-A-G

http://identifiers.org/hco/21/GRCh38#37456021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94452557-C-A

37456301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 94452755-A-G

37456318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94452771-T-C

37456545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94452996-G-A

37456580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94453034-C-T

http://identifiers.org/hco/21/GRCh38#37456906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94453326-A-C

37457027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94453449-T-C

37457848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94454183-T-G

37460580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94455249-G-A

37460580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94455249-G-T

37460893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94455669-G-A

37462117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94456805-G-C

37462137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94456816-A-T

37462396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94457023-G-A

37462608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94457234-G-A

37462775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94457338-A-G

37463033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94457559-A-G

37463113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94457633-T-C

37463114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94457634-G-A

37463361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94457787-T-G

37463451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94457883-C-T

http://identifiers.org/hco/21/GRCh38#37463649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#94458061-C-A

37463649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, undefined
orthologous variants: 94458061-C-T

37463715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94458119-C-T

37463971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94458386-C-G

37463971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94458386-C-T

37464230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94458602-T-C

37464331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94458699-G-T

37464425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94458779-G-A

37464907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94459282-G-T

37472003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94459561-A-G

37472062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94459623-G-T

37472079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94459669-A-G

37472534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94460211-G-T

37472567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94460243-A-G

37472621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94460297-T-C

37472621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron variant
orthologous variants: 94460297-T-G

37472917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94460587-G-A

37472917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94460587-G-T

37473009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94460663-G-A

37473009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94460663-G-C

37473009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94460663-G-T

37473275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94460860-A-G

37473275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94460860-A-T

http://identifiers.org/hco/21/GRCh38#37473496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94461057-C-A

37473496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461057-C-T

37473503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461064-G-A

37473763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461320-T-C

37473875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461414-G-A

37473987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461532-T-C

37474163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461709-A-G

37474759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462470-G-A

37474852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462561-G-A

37474930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462643-G-T

37474942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462653-G-A

37476370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94463044-G-A

37476504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94463171-G-A

37477863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464213-T-C

37479136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94465796-T-A

37479136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94465796-T-C

http://identifiers.org/hco/21/GRCh38#37479398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94466022-C-A

37479447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466072-A-T

37479996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466186-G-A

http://identifiers.org/hco/21/GRCh38#37480133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94466314-A-C

37480623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466760-G-A

37480793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 94466930-T-A

37486341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94469549-G-T

37486444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94469641-G-T

37489347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471385-A-T

http://identifiers.org/hco/21/GRCh38#37489436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94471450-C-A

http://identifiers.org/hco/21/GRCh38#37489479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94471482-C-A

37490060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472036-T-A

37490060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472036-T-C

37490078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472060-G-T

37490158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472143-A-G

37490473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472460-T-A

37490473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472460-T-C

37490856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472689-T-C

http://identifiers.org/hco/21/GRCh38#37491073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94472876-C-A

37492801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474026-C-G

37493115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94474294-T-C

37493222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474364-G-A

37493242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474384-T-C

37493278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474426-A-G

37493469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474625-G-C

37493469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474625-G-T

37493490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474652-A-G

37496385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94478610-A-G

37496413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94478638-A-G

37496617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94478814-G-A

37496685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94478863-A-T

37497284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94479674-C-T

37501671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94482505-T-A

37502201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94483165-T-C

37502241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94483201-G-T

37502551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94483471-G-T

37503051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94483796-A-G

37503058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94483803-C-T

37503095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94483831-G-A

37503095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94483831-G-T

37503425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484167-G-A

37503425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484167-G-T

37503709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484422-T-G

37503750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484466-T-C

37503762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484479-A-T

37503921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484627-G-T

http://identifiers.org/hco/21/GRCh38#37503973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94484673-A-C

37503973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484673-A-G

http://identifiers.org/hco/21/GRCh38#37504050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94484730-C-A

37504050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484730-C-T

37504247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484881-C-T

37504272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484883-G-T

37504900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94485516-A-G

37505072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94485690-T-C

http://identifiers.org/hco/21/GRCh38#37505077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94485696-C-A

37505077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94485696-C-T

37505166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94485799-G-A

37505166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94485799-G-T

37505615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486229-G-A

37505615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486229-G-T

37505654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486268-A-G

http://identifiers.org/hco/21/GRCh38#37505700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94486629-C-A

37505700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486629-C-G

37505700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486629-C-T

37505757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486699-A-G

37505773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486715-G-A

37506044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94487287-G-A

37506044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94487287-G-C

37506044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94487287-G-T

37506077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94487316-G-A

37506279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94487508-G-C

37506305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94487528-T-C

37506451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94487647-G-A

37506451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94487647-G-C

37506451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94487647-G-T

37506843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94488289-G-A

37506843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94488289-G-C

37506967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94488410-T-G

37506982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94488425-G-T

37507052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94488483-C-T

37507153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94488542-T-C

http://identifiers.org/hco/21/GRCh38#37507467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94488737-A-C

http://identifiers.org/hco/21/GRCh38#37507553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94488821-C-A

37507553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94488821-C-T

37507670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94488922-C-T

37512072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94492601-C-T

37512078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94492607-C-T

37512983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94493504-G-T

37513714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494241-T-C

37513867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494391-A-G

37513905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494427-T-C

37513927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494448-T-A

37513927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494448-T-C

http://identifiers.org/hco/21/GRCh38#37514222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94494740-C-A

37514222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494740-C-T

37514284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494802-A-G

37514297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494815-T-C

37514337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494854-A-G

37514362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494879-G-A

37514405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94494923-A-G

37514532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94495077-C-T

37514550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94495106-T-C

http://identifiers.org/hco/21/GRCh38#37514662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94495209-C-A

37514790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94495325-T-C

37514913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94495458-G-A

37514913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94495458-G-T

37515076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94495620-G-A

37515541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94496056-C-T

37515599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94496108-A-G

37515738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94496239-A-G

http://identifiers.org/hco/21/GRCh38#37515768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94496264-A-C

37516273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94496707-A-G

http://identifiers.org/hco/21/GRCh38#37516285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94496719-C-A

37516285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3091
most severe consequence: 3 prime UTR variant
orthologous variants: 94496719-C-T