27133512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447097-A-G

27133513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-C-G

27133534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-A-G

27133550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447059-A-G

http://identifiers.org/hco/16/GRCh38#27133554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447055-A-C

27133575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447034-C-T

27133576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447033-T-C

27133577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-A

27133577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-C

27133579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447030-C-G

http://identifiers.org/hco/16/GRCh38#27133590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447019-C-A

27133590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447019-C-G

27133590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447019-C-T

http://identifiers.org/hco/16/GRCh38#27133607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447002-C-A

27133607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40447002-C-T

27133611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446998-G-A

27133611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446998-G-C

27133611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446998-G-T

27133613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446996-G-A

27133613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446996-G-C

27133613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446996-G-T

27133616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446993-G-T

27133621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446988-G-A

27133621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446988-G-T

27133622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446987-T-C

http://identifiers.org/hco/16/GRCh38#27133631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446978-C-A

27133631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446978-C-T

27133638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-T-G

27133641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446968-A-G

27133655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446954-G-A

http://identifiers.org/hco/16/GRCh38#27133660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446949-C-A

27133672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-A

27133672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-T

27133675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446934-A-G

27133679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446930-T-C

27133719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-T-C

http://identifiers.org/hco/16/GRCh38#27133734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446874-C-A

27133734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446874-C-T

27133772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446836-T-A

27133772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446836-T-C

http://identifiers.org/hco/16/GRCh38#27133784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446824-C-A

27133784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446824-C-T

27133802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-T-A

27133802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-T-C

27133802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-T-G

27133877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446731-T-A

27133877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446731-T-G

http://identifiers.org/hco/16/GRCh38#27133901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446709-C-A

27133901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446709-C-G

27133901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446709-C-T

http://identifiers.org/hco/16/GRCh38#27133920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446690-C-A

27133920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446690-C-T

27133924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446686-A-G

27133924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446686-A-T

http://identifiers.org/hco/16/GRCh38#27133925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446685-C-A

27133925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446685-C-T

27133934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446676-T-C

27133971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446639-T-C

http://identifiers.org/hco/16/GRCh38#27133973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446637-C-A

27133973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446637-C-T

27133990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446620-T-A

27133990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446620-T-C

http://identifiers.org/hco/16/GRCh38#27134023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446587-C-A

27134023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446587-C-T

27134052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446558-G-T

27134053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446557-G-A

27134064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-A-G

http://identifiers.org/hco/16/GRCh38#27134065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446545-C-A

27134065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446545-C-G

27134065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446545-C-T

http://identifiers.org/hco/16/GRCh38#27134077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446533-C-A

27134077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446533-C-T

27134085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446525-A-G

http://identifiers.org/hco/16/GRCh38#27134105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446505-C-A

27134105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446505-C-T

http://identifiers.org/hco/16/GRCh38#27134117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446493-C-A

27134117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446493-C-T

27134132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446478-G-A

27134132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446478-G-T

27134151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446459-T-A

27134151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446459-T-C

27134154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446456-A-G

27134154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446456-A-T

27134164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446446-G-A

27134164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446446-G-C

27134164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446446-G-T

27134166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446444-T-A

27134166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446444-T-C

27134172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-G-A

27134172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-G-T

http://identifiers.org/hco/16/GRCh38#27134173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446437-C-A

27134173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446437-C-T

27134178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446432-A-G

27134179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446431-A-G

27134179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446431-A-T

http://identifiers.org/hco/16/GRCh38#27134186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446424-C-A

27134186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446424-C-T

27134188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-A-G

27134188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-A-T

http://identifiers.org/hco/16/GRCh38#27134190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446420-C-A

27134190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446420-C-T

27134191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446419-A-G

27134192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446418-G-A

27134192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446418-G-T

27134197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446413-G-A

27134197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446413-G-T

http://identifiers.org/hco/16/GRCh38#27134203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446407-C-A

27134203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446407-C-T

http://identifiers.org/hco/16/GRCh38#27134207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446403-C-A

27134207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446403-C-T

27134215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-T-A

27134215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-T-C

27134218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446392-T-A

27134218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446392-T-C

27134218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446392-T-G

27134220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446390-A-T

27134226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446384-T-C

27134226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446384-T-G

http://identifiers.org/hco/16/GRCh38#27134236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446374-C-A

27134236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446374-C-T

27134248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-A

27134248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-C

27134248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-T

27134251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446359-A-G

27134259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446351-A-G

27134259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446351-A-T

http://identifiers.org/hco/16/GRCh38#27134282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446328-C-A

27134282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446328-C-T

http://identifiers.org/hco/16/GRCh38#27134295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446315-A-C

27134295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446315-A-G

27134317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446293-T-A

27134317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446293-T-C

27134317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446293-T-G

27134668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446249-A-G

27134669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446248-A-G

27134669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446248-A-T

http://identifiers.org/hco/16/GRCh38#27134677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446240-C-A

27134677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446240-C-T

27134678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-A

27134678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-C

27134678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-G

27134696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446221-T-C

27134705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446212-T-C

http://identifiers.org/hco/16/GRCh38#27134729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446188-C-A

27134729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446188-C-T

http://identifiers.org/hco/16/GRCh38#27134730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446187-C-A

27134730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446187-C-T

http://identifiers.org/hco/16/GRCh38#27134735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446182-A-C

27134735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446182-A-G

27134735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446182-A-T

27134738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446179-A-G

27134738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446179-A-T

27134741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446176-T-A

27134741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446176-T-G

27134752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446165-T-C

http://identifiers.org/hco/16/GRCh38#27134775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446141-C-A

27134775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-C-T

27134776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446140-T-A

27134776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446140-T-C

http://identifiers.org/hco/16/GRCh38#27134777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446139-C-A

27134777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446139-C-G

27134777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446139-C-T

27134786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-A

27134786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-C

27134786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-T

http://identifiers.org/hco/16/GRCh38#27134787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446129-C-A

27134787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-C-T

http://identifiers.org/hco/16/GRCh38#27134788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446128-C-A

27134788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446128-C-T

27134794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446122-T-C

27134808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446108-T-C

27134830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446086-G-A

27134830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446086-G-T

27134832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-A-G

27134839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446077-A-G

http://identifiers.org/hco/16/GRCh38#27134855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446061-C-A

27134855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-C-G

27134855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-C-T

http://identifiers.org/hco/16/GRCh38#27134856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446060-C-A

27134856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446060-C-T

27134857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446059-T-C

27134863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-A

27134863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-C

27134863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-T

27134873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446043-T-C

27134881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446035-T-C

27134883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-G-A

27134883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-G-C

27134883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-G-T

27134884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446032-A-G

27134889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446027-G-A

27134889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446027-G-T

http://identifiers.org/hco/16/GRCh38#27134893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446023-C-A

27134893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446023-C-G

27134893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446023-C-T

27134894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446022-T-C

27134894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446022-T-G

27134902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446014-G-T

27134913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446003-G-A

27134913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446003-G-T

27134914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446002-A-G

27134914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40446002-A-T

27134920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445996-A-G

http://identifiers.org/hco/16/GRCh38#27134926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445990-C-A

27134926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445990-C-T

27134938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445978-T-A

27134938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445978-T-C

http://identifiers.org/hco/16/GRCh38#27134949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445967-C-A

27134949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445967-C-T

http://identifiers.org/hco/16/GRCh38#27134956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445960-A-C

27134956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445960-A-T

http://identifiers.org/hco/16/GRCh38#27134960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445956-C-A

27134960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-C-T

27134962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445954-A-G

27134973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445943-A-G

http://identifiers.org/hco/16/GRCh38#27134974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445942-C-A

27134974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445942-C-G

27134974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445942-C-T

http://identifiers.org/hco/16/GRCh38#27134978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445938-C-A

27134985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445931-A-G

http://identifiers.org/hco/16/GRCh38#27134995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445921-C-A

27134998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445918-T-C

http://identifiers.org/hco/16/GRCh38#27135006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445910-C-A

27135006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445910-C-T

27135008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445908-A-G

27135008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445908-A-T

27135010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445906-G-A

27135010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445906-G-C

27135010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445906-G-T

http://identifiers.org/hco/16/GRCh38#27135025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445891-C-A

27135025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-C-G

27135025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-C-T

27135052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445864-T-C

27135060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445856-T-C

27135067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445849-G-A

27135067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445849-G-T

27135069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445847-T-A

27135069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445847-T-C

http://identifiers.org/hco/16/GRCh38#27135070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445846-C-A

27135076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445840-T-A

27135076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445840-T-C

27135100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445816-A-G

27135104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-A

27135104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-T

27135147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-T

27135173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37916
most severe consequence: non coding transcript exon variant
orthologous variants: 40445768-T-G