132296111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178463-G-C

132296111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178463-G-T

132296131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178443-T-C

132296131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178443-T-G

132296169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178408-G-C

http://identifiers.org/hco/6/GRCh38#132296232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24178337-A-C

132296358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178236-G-T

http://identifiers.org/hco/6/GRCh38#132296415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24178196-C-A

132296513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178106-G-A

132296513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178106-G-T

132296514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178105-G-A

132296540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24178086-T-G

http://identifiers.org/hco/6/GRCh38#132296571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24178066-C-A

132296738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177912-G-T

132296760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177890-T-C

132296793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177860-T-C

132296813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177857-G-A

132296813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177857-G-T

132296861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177819-A-G

132296958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177727-T-A

132297029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177657-G-T

132297131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177542-G-T

132297132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177541-T-C

132297141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177532-A-G

132297142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3 prime UTR variant
orthologous variants: 24177531-C-T

132297167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24177511-T-C

132297167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24177511-T-G

132297223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24177455-C-G

132297277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24177401-G-T

132297346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24177334-T-C

132297352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24177328-T-C

132297379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176670-G-A

132297384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176665-T-C

132297454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176595-A-G

132297467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176581-G-A

132297467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176581-G-C

132297467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176581-G-T

132297477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176568-G-A

132297487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176556-A-G

132297535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176511-G-T

132297634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176378-G-A

http://identifiers.org/hco/6/GRCh38#132297683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24176326-C-A

132297683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176326-C-T

http://identifiers.org/hco/6/GRCh38#132297691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24176318-C-A

132297719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176291-T-C

132297756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24176254-T-C

http://identifiers.org/hco/6/GRCh38#132297821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24176186-A-C

132297872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24176135-T-C

132298060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24175960-C-G

132298060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24175960-C-T

http://identifiers.org/hco/6/GRCh38#132298098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24175926-C-A

132298415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24175243-T-C

132298577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24175084-C-T

132299486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174870-T-A

http://identifiers.org/hco/6/GRCh38#132299493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24174863-A-C

132299493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174863-A-G

132299679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174731-G-A

132299683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174727-A-G

132299706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174705-A-G

132299706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174705-A-T

132299787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174625-C-G

132299795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174615-G-C

http://identifiers.org/hco/6/GRCh38#132299838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24174571-A-C

132300037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174407-T-C

132300080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174363-G-T

132300131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174304-G-T

132300176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174261-G-T

132300202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174235-T-C

132300289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174160-T-A

132300289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174160-T-C

132300382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24174068-G-T

http://identifiers.org/hco/6/GRCh38#132300585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24173807-A-C

132300585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24173807-A-G

132300703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24173693-A-G

132300816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24173587-T-G

132301017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24173424-T-G

132301190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24173139-G-A

132301275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24173032-T-C

132301337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24172970-T-C

132301973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24172309-T-C

132302157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24172139-A-T

132302212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24172085-G-T

132302236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24172062-C-T

132302241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24172057-C-T

132302504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24171790-A-G

132302504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24171790-A-T

132302516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24171778-T-C

http://identifiers.org/hco/6/GRCh38#132302560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24171734-C-A

132302622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24171561-T-C

http://identifiers.org/hco/6/GRCh38#132302664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24171527-C-A

132302664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24171527-C-T

132302810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24171361-C-G

132302834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24171337-G-C

132302914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24171274-C-T

132311290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24168495-T-C

132311332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24168458-T-G

132311506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24168310-T-C

http://identifiers.org/hco/6/GRCh38#132311580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24168242-A-C

132311631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24168198-C-T

132311757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24168073-T-C

132311843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24167989-T-C

132311906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24167927-G-A

132312070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24167654-A-G

132312070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24167654-A-T

132312176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24167540-G-A

132312193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24167524-T-C

132312285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24167424-A-T

http://identifiers.org/hco/6/GRCh38#132312610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24167109-C-A

132312610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24167109-C-T

132313441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24165097-A-G

132313540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24165012-T-C

132314006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24164885-T-C

132314096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24164798-C-T

132314105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24164789-T-C

132314171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24164718-C-T

132314392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24164507-T-C

132314544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24164190-C-T

132315073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24163517-G-A

132315122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24163468-T-G

132315212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24163380-A-G

132315486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24163170-A-G

132315874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24162820-T-A

132315874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24162820-T-C

132319731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24161594-T-A

132319780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24161553-T-A

132319798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24161535-T-C

http://identifiers.org/hco/6/GRCh38#132319917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24161420-C-A

132320188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24161151-T-C

132320318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24161020-G-A

132320416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160918-C-T

http://identifiers.org/hco/6/GRCh38#132320483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24160860-C-A

132320483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160860-C-G

132320506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160838-G-T

132320519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160825-T-A

132320519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160825-T-C

132320519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160825-T-G

132320520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160824-T-G

132320545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160800-A-G

132320586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160750-T-C

132320692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24160648-A-G

132320716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160626-A-G

http://identifiers.org/hco/6/GRCh38#132320743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24160599-C-A

132320743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160599-C-G

132320782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160560-G-A

132320782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160560-G-C

132320782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160560-G-T

132320801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160541-T-C

132320870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160480-T-C

132321381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24160264-G-T

132321627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24159992-T-C

http://identifiers.org/hco/6/GRCh38#132321646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24159948-C-A

132321891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24159666-T-C

132322077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24159507-A-G

132322169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24159402-A-G

http://identifiers.org/hco/6/GRCh38#132322622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24158696-C-A

132322785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24158544-C-T

132323267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24158099-A-G

132323273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24158093-A-G

132323482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24157892-T-G

132323818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24157586-G-A

132323818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24157586-G-T

http://identifiers.org/hco/6/GRCh38#132323849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24157559-C-A

132323884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24157529-G-T

132323950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24157461-G-A

http://identifiers.org/hco/6/GRCh38#132323976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24157435-A-C

132323989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24157422-G-C

132323989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24157422-G-T

http://identifiers.org/hco/6/GRCh38#132324152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24157273-C-A

132324321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24157127-C-T

132324540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24156927-C-T

132327207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24156596-C-T

132327301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24156514-G-A

132327785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24156053-C-T

132328024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24155830-G-T

132328147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155701-C-T

132328190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155661-A-G

132328191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155660-T-G

132328201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155649-T-C

132328222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155629-C-T

132328237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155618-G-A

132328237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155618-G-T

132328280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155576-A-T

132328293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155563-T-A

132328293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155563-T-C

132328296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155560-G-A

132328296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155560-G-T

http://identifiers.org/hco/6/GRCh38#132328410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24155446-C-A

132328410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155446-C-G

132328410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155446-C-T

132328416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 24155440-T-G

132328425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24155431-A-G

132328508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: synonymous variant
orthologous variants: 24155348-A-T

132328515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24155341-T-C

http://identifiers.org/hco/6/GRCh38#132328654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24155202-C-A

132328654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155202-C-T

132328660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155196-A-T

132328790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155068-G-A

132328790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155068-G-C

132328790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24155068-G-T

http://identifiers.org/hco/6/GRCh38#132330115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24154465-C-A

132330721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24154333-T-A

132330734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24154320-T-C

132330853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24154210-T-A

132330932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24154159-G-A

132330957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24154135-A-T

http://identifiers.org/hco/6/GRCh38#132330969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24154123-A-C

132331200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24153894-G-A

132331258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24153836-T-G

132331459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24153662-A-G

132331596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24153540-C-T

132331600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24153536-C-T

132331648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24153477-T-A

132331784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24153342-A-G

http://identifiers.org/hco/6/GRCh38#132331916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24153227-A-C

http://identifiers.org/hco/6/GRCh38#132331982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24153171-C-A

http://identifiers.org/hco/6/GRCh38#132332083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24153082-C-A

132335487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24152874-T-G

132335619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24152766-C-T

132335781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24152623-T-G

132336002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24152449-A-G

132336204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24152247-G-A

132336594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24152062-T-C

132336777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24151889-G-A

http://identifiers.org/hco/6/GRCh38#132337157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24151568-A-C

132337236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24151515-A-G

132337344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24151423-G-T

http://identifiers.org/hco/6/GRCh38#132337412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24151380-C-A

132341551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24150478-C-T

http://identifiers.org/hco/6/GRCh38#132341629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24150398-A-C

132341630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24150397-T-C

http://identifiers.org/hco/6/GRCh38#132341697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24150330-C-A

132341833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24150197-T-C

132342193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24150043-G-T

132342351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24149986-C-T

132342441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24149898-A-G

132342548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24149776-A-G

132342618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24149610-T-C

132343004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24149279-C-T

132345855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24148181-A-G

132345957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24148099-G-A

132346047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24148004-G-T

132346599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24147450-A-G

132346617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24147434-C-T

132346661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24147389-G-A

132346661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24147389-G-T

http://identifiers.org/hco/6/GRCh38#132346711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24147343-C-A

132346712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24147342-A-G

132346867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24147176-T-C

132346920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24147134-A-G

132346931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24147123-T-C

132348135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24146932-C-T

132348506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24146318-A-G

132348635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24146204-A-G

132348816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24146013-C-G

132348819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24146010-A-G

132348846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24145983-G-A

132348946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24145888-T-C

http://identifiers.org/hco/6/GRCh38#132356391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24144379-A-C

132356816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24143992-T-A

132356936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24143860-T-G

132356945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24143837-A-G

http://identifiers.org/hco/6/GRCh38#132356972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24143760-A-C

http://identifiers.org/hco/6/GRCh38#132357022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24143689-C-A

http://identifiers.org/hco/6/GRCh38#132357058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24143652-A-C

132357110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24143588-C-T

132357360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24143349-C-T

132357375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24143334-T-C

132357815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24142948-G-A

132357991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24142786-A-G

132358375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24142455-C-T

132358422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24142412-T-C

132359062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: -T-A

132359062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: -T-C

132359830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24141019-T-A

132360929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140481-T-A

132360968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140448-C-T

132360978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140438-T-C

132361050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140365-A-G

http://identifiers.org/hco/6/GRCh38#132361182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24140217-C-A

132361200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140199-A-G

132361248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140156-T-G

132361276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140122-G-A

132361276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140122-G-T

132361342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24140066-T-A

http://identifiers.org/hco/6/GRCh38#132361762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24138560-A-C

132362164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24138224-G-T

http://identifiers.org/hco/6/GRCh38#132362513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24137896-A-C

132362513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137896-A-G

http://identifiers.org/hco/6/GRCh38#132362604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24137812-A-C

132362715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137702-C-T

132362779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137618-T-C

132362968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137420-G-A

132363253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137155-A-T

132363282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137126-C-T

132363306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137101-T-G

132363371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137038-T-A

132363371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24137038-T-C

132363884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24136550-A-G

132364085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24136355-A-T

132364227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24136215-G-T

132364484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135948-G-A

132364484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135948-G-T

132364610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135846-C-T

132364741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135758-A-T

132364844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135668-C-G

132364844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135668-C-T

132364908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135606-T-C

132365029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135502-G-A

132365272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135289-G-A

132365312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135260-C-T

132365321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135251-A-G

132365541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135051-A-T

132365553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24135039-A-G

132365801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, undefined
orthologous variants: 24134798-G-A

132365801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron_variant, undefined
orthologous variants: 24134798-G-T

132365865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134734-A-G

132366031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134527-A-G

132366254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134382-A-G

132366431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134230-A-G

http://identifiers.org/hco/6/GRCh38#132366434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24134227-A-C

132366466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134207-G-T

132366496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134177-C-G

132366496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134177-C-T

132366515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134153-A-G

132366630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24134047-T-G

132366706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24133980-T-G

132366828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24133860-T-G

132366906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24133783-C-G

132366948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24133746-A-G

132366951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24133743-C-T

132367080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24133638-T-C

132367082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24133636-G-A

132367226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24133374-G-T

http://identifiers.org/hco/6/GRCh38#132367447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24133000-C-A

132367473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24132976-A-G

132367734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24132701-A-T

132367754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24132681-C-T

132367867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24132575-T-C

132368036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24132443-G-A

132368282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24132193-A-G

132368439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24132010-G-A

http://identifiers.org/hco/6/GRCh38#132368455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24131997-A-C

132368455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24131997-A-G

132368513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24131815-T-A

132368664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24131672-C-T

132370144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24131102-G-A

http://identifiers.org/hco/6/GRCh38#132370260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24130990-C-A

132370462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24130789-C-T

132370609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24130654-C-T

132370657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24130612-T-C

132371016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24130305-G-A

132371045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24130278-A-G

132371102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24130222-A-G

132371330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24130013-G-A

132371342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24130001-C-T

132371667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129725-T-C

132371712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129682-G-A

132371712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129682-G-C

132371712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129682-G-T

132371738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129659-T-A

132371837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129557-T-C

132371844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129550-G-A

132371949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129470-C-T

132372178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129253-T-A

132372292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129143-A-T

http://identifiers.org/hco/6/GRCh38#132372387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24129095-C-A

132372489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24129024-C-T

132372526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128987-C-T

http://identifiers.org/hco/6/GRCh38#132372548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24128964-A-C

132372548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128964-A-T

132372574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128945-A-G

132372586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128933-A-G

132372639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24128880-G-A

132372639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24128880-G-C

http://identifiers.org/hco/6/GRCh38#132372769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24128750-A-C

132372785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128736-T-A

132372785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128736-T-G

http://identifiers.org/hco/6/GRCh38#132372796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24128725-C-A

132372906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24128450-C-T

132373045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128312-T-C

http://identifiers.org/hco/6/GRCh38#132373049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24128308-C-A

132373090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128267-A-G

132373094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128263-G-A

132373094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128263-G-T

132373121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128236-G-A

132373121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24128236-G-T

132373503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24121438-C-T

http://identifiers.org/hco/6/GRCh38#132373906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24120975-C-A

http://identifiers.org/hco/6/GRCh38#132373932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24120950-C-A

132373932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24120950-C-T

132374559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24120364-T-C

132374710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24120203-G-A

132374710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24120203-G-T

132374740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24120173-T-C

132374740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24120173-T-G

132374894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 24119980-T-G

132374964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 24119910-G-T

132374988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 24119886-A-T

132375083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24119796-T-C

132375083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24119796-T-G

http://identifiers.org/hco/6/GRCh38#132375104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24119775-C-A

132375104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24119775-C-G

132375104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24119775-C-T

132375121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24119763-T-C

132375188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24119715-A-G

132375284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24119636-T-A

132375287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24119633-C-T

132376188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118909-A-G

132376203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118894-C-T

132376260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118818-G-T

132376399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118691-G-T

132376421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118672-T-C

http://identifiers.org/hco/6/GRCh38#132376897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24118521-A-C

132376939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118492-C-T

132377031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118408-T-G

http://identifiers.org/hco/6/GRCh38#132377278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24118182-A-C

132377278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118182-A-T

132377298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24118163-A-G

132377695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24117833-T-C

http://identifiers.org/hco/6/GRCh38#132378372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24117182-C-A

132378455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24117102-T-G

132378638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24116942-A-G

132379030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24115966-A-T

132379106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24115889-G-T

132379129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24115866-T-G

132379198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24115806-T-C

132379266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24115736-T-C

132379670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24115475-C-T

132380140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24115250-C-G

132380269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24115115-G-A

132380435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24114947-C-G

132380559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24114829-T-C

132380673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24114715-T-A

132380728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24114659-T-A

132380728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24114659-T-C

132380914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24114504-C-T

http://identifiers.org/hco/6/GRCh38#132381377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24114303-C-A

132381486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24114203-A-T

132381490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24114199-T-C

http://identifiers.org/hco/6/GRCh38#132381802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24113953-A-C

132381919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24113843-A-G

132381969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24113767-T-C

132381974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24113762-T-C

132382229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24112518-T-G

132382675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24112064-A-T

132382715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24112020-T-C

132382807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24111925-T-C

http://identifiers.org/hco/6/GRCh38#132383208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24111488-A-C

132383208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24111488-A-T

http://identifiers.org/hco/6/GRCh38#132383453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24111253-A-C

132383566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24111183-T-A

132383597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24111157-C-T

132383753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24111024-T-A

132383757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24111020-A-G

132387872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24108896-C-G

132387906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24108859-C-T

132388256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24108571-C-T

132388257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24108570-C-T

132388516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24108299-C-T

132388676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24108148-G-A

132388760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24108069-T-C

132388911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24107923-T-C

132388917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24107917-T-A

132388966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24107869-G-A

132388966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24107869-G-T

132389476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24107566-T-C

132389508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24107533-T-C

132389565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24107481-G-C

http://identifiers.org/hco/6/GRCh38#132389608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24107441-A-C

132389842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24107157-T-C

http://identifiers.org/hco/6/GRCh38#132389870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24107122-A-C

http://identifiers.org/hco/6/GRCh38#132390315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24106823-C-A

132390327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24106811-C-T

132390433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24106725-C-T

http://identifiers.org/hco/6/GRCh38#132390544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24106619-C-A

132390544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24106619-C-T

132390643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24106501-G-A

132390659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24106485-G-A

http://identifiers.org/hco/6/GRCh38#132390672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24106472-C-A

http://identifiers.org/hco/6/GRCh38#132390678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24106466-C-A

132390715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24106431-T-C

132390810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24106351-G-A

http://identifiers.org/hco/6/GRCh38#132391121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24106117-C-A

132391135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24106106-G-A

132391135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24106106-G-T

http://identifiers.org/hco/6/GRCh38#132391645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24105052-C-A

132391820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24104882-G-A

132391820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24104882-G-T

132391903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24104792-T-C

132391996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24104704-G-A

132391996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24104704-G-C

132391996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24104704-G-T

132392006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24104694-T-C

132392036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 24104665-G-A

132392036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 24104665-G-T

http://identifiers.org/hco/6/GRCh38#132392209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24104516-C-A

132392209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24104516-C-T

132392225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 24104500-G-A

http://identifiers.org/hco/6/GRCh38#132392316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24104404-C-A

132392365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24104353-G-T

132392411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24104309-G-A

132392411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24104309-G-T

http://identifiers.org/hco/6/GRCh38#132392488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24104232-A-C

132392495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24104225-C-T

132392509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24104211-G-A

132392576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24104161-G-A

132392755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24103967-T-C

132392818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24103904-T-C

132393053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24103301-G-A

132397164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102832-A-G

132397290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102667-T-A

132397343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102609-C-T

132397344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102608-C-T

132397420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102532-T-C

132397441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102511-G-A

132397580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102376-G-A

132397630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102326-G-A

132397630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102326-G-C

132397634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102322-G-A

http://identifiers.org/hco/6/GRCh38#132397636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24102320-C-A

132397636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102320-C-G

132397650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102306-G-A

132397859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102212-T-C

132398336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102031-T-C

132398341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24102025-T-C

132398460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24101928-G-A

132398483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24101906-C-T

132398488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24101901-G-A

http://identifiers.org/hco/6/GRCh38#132399395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24101345-A-C

http://identifiers.org/hco/6/GRCh38#132399576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24101192-A-C

132399674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24101094-A-G

132399773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24101012-T-G

132399933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100860-T-A

132399933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100860-T-G

132399986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100824-T-C

132400075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100727-T-C

132400097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100710-A-G

132400199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100625-T-C

132400299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100528-A-G

132400599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100268-T-A

132400632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24100235-G-A

132400940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099967-C-T

132401003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099898-G-A

http://identifiers.org/hco/6/GRCh38#132401019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24099882-C-A

132401019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099882-C-G

132401019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099882-C-T

132401022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099879-G-T

132401030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099871-G-A

132401030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099871-G-C

132401030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099871-G-T

132401131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099797-G-A

132401131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099797-G-C

132401135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: intron variant
orthologous variants: 24099793-G-A

http://identifiers.org/hco/6/GRCh38#132401290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24099636-C-A

132401290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24099636-C-T

http://identifiers.org/hco/6/GRCh38#132401368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24099558-C-A

132401368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24099558-C-G

132401368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24099558-C-T

132401393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: synonymous variant
orthologous variants: 24099533-G-A

132401393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24099533-G-C

132401393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24099533-G-T

132401407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: missense variant
orthologous variants: 24099519-A-G

http://identifiers.org/hco/6/GRCh38#132401444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24099488-C-A

132401444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21063
most severe consequence: 5 prime UTR variant
orthologous variants: 24099488-C-T