135234166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595065-C-T

135234231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595158-T-C

135234258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595185-A-G

135234282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595209-T-C

135234381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595296-G-A

135234381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595296-G-C

135234381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595296-G-T

135234428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595342-G-C

135234428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595342-G-T

135234432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595346-G-A

135234499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68595411-A-T

http://identifiers.org/hco/8/GRCh38#135234530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68595441-C-A

135234530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68595441-C-G

135234530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68595441-C-T

135234558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68595470-G-A

135234587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68595497-T-C

http://identifiers.org/hco/8/GRCh38#135234600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68595515-C-A

135234600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595515-C-T

135234611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595525-A-G

135234627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595541-G-A

135234627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595541-G-T

135234685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595569-C-T

http://identifiers.org/hco/8/GRCh38#135234691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68595575-C-A

135234691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595575-C-T

135234759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595641-G-C

135234790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595672-A-G

135235903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68596308-G-A

135236248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68597178-A-G

135236270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68597200-T-G

135236335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68597252-C-T

135236558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68597456-C-T

135236646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68597538-A-G

135241843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68598557-A-G

135241900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68598607-T-C

135252645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68602802-T-G

135252738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68602891-G-T

135254111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603358-A-T

135254228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603485-T-A

135254374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603639-C-T

135254421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603664-G-A

135254468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603707-T-C

135254522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603745-T-C

135254667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603893-T-G

http://identifiers.org/hco/8/GRCh38#135254675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68603901-A-C

135254675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603901-A-G

135254745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603969-A-G

135254989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68604170-C-T

135255117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68604300-A-G

135255132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68604314-C-T

135255402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68604576-C-T

135255420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68604593-A-G

135255442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68604632-G-A

135257128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605719-C-T

http://identifiers.org/hco/8/GRCh38#135257154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68605745-C-A

135257223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605810-T-G

135257404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606001-A-G

135257404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606001-A-T

135257427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606026-G-A

135257701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606332-A-T

135257778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606396-C-G

135257778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606396-C-T

135257787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606404-G-T

135257873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606553-A-T

135257959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606634-C-T

135258050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606718-T-A

135258084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606740-T-C

135258305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606956-A-G

135258474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607130-G-A

135258474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607130-G-T

135258567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607205-G-A

135258573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607211-G-T

135258626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607260-G-T

135258691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607331-G-C

135258741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607381-C-G

135258994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607652-T-A

135272669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607774-G-T

135272789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68607916-T-C

135272954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608055-T-A

135272954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608055-T-C

135272966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608067-G-T

135272968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608069-G-A

135273200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608299-G-A

135273364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608455-G-A

135273471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608567-T-C

135273528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608607-C-T

135273552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608627-A-G

135273702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608727-T-C

135273709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608734-C-T

135273788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608811-C-G

135273819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608835-C-T

135273892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608908-G-A

135273899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608914-A-G

135273902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608917-G-C

135273902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608917-G-T

135273945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608954-T-C

135274247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609217-G-A

135274268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609238-C-G

135274724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609356-A-G

135275057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609656-G-A

135275238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609836-G-T

135275369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609956-C-T

135275753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68610333-A-G

135275820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68610407-A-G

135275898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68610490-A-G

135275922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68610509-C-T

135275923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68610510-T-G

135277577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68611591-G-A

135277577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68611591-G-C

http://identifiers.org/hco/8/GRCh38#135277614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68611621-C-A

135277614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68611621-C-T

135277941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68611885-C-T

135278001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68611966-T-C

135278075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612025-G-T

135278108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612050-C-G

135278201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612124-C-T

http://identifiers.org/hco/8/GRCh38#135278214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68612137-C-A

135278265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612179-C-T

135278273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612187-G-A

135278295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612201-T-C

135278440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612368-G-A

135278577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612503-T-A

135278577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612503-T-C

http://identifiers.org/hco/8/GRCh38#135278673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68612594-C-A

http://identifiers.org/hco/8/GRCh38#135278709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68612622-A-C

135278858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612762-A-T

135278864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68612768-G-T

135279158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68613042-T-C

135279201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68613081-C-T

http://identifiers.org/hco/8/GRCh38#135279624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68614508-C-A

135279624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68614508-C-T

http://identifiers.org/hco/8/GRCh38#135279634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68614518-C-A

135279634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68614518-C-T

135279645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68614529-A-G

135279771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68614655-T-C

http://identifiers.org/hco/8/GRCh38#135280094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68615730-C-A

135280314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68616136-T-C

135280668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68616539-G-T

http://identifiers.org/hco/8/GRCh38#135280856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68616699-C-A

http://identifiers.org/hco/8/GRCh38#135281030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68616873-C-A

135281037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68616880-G-C

http://identifiers.org/hco/8/GRCh38#135281082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68616923-A-C

http://identifiers.org/hco/8/GRCh38#135281177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68617018-C-A

http://identifiers.org/hco/8/GRCh38#135282037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68618928-A-C

135282082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68618973-G-A

135282096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68618987-G-A

135282173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619075-G-A

135282173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619075-G-T

135282452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619337-G-A

135282860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619733-G-A

135283057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619918-G-A

135283256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68620128-A-G

135286533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68623294-T-A

135286533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68623294-T-C

135286535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68623296-C-G

135286535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68623296-C-T

135286544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68623305-A-G

135286545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68623306-T-A

135286545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68623306-T-C

http://identifiers.org/hco/8/GRCh38#135286660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68623415-C-A

135286877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68623641-G-A

135287254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624037-C-T

http://identifiers.org/hco/8/GRCh38#135287321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68624099-A-C

135287424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624218-C-T

135287478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624272-G-A

135287505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624301-C-T

135287738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624528-A-T

135287795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624557-G-A

135287909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624645-G-C

135287960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624694-A-G

135287960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624694-A-T

http://identifiers.org/hco/8/GRCh38#135287965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68624699-C-A

135287965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624699-C-T

135287966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624700-T-C

http://identifiers.org/hco/8/GRCh38#135287988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68624722-C-A

135288072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624805-C-G

135288072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624805-C-T

135288123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624861-G-A

135288126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624864-C-G

135288145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68624879-A-T

135288416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625051-G-A

http://identifiers.org/hco/8/GRCh38#135288632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68625402-A-C

135288796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625538-C-T

135288843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625582-G-A

135288875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625614-C-G

135289113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625850-T-C

135289191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625924-T-C

135289196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625930-T-A

135289298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626031-C-G

135289298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626031-C-T

135289330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626053-A-G

135289627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626696-A-G

135289685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626742-T-C

135290304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627356-C-T

135290305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627357-G-A

135290357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627400-C-T

135290486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627533-C-T

135290490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627537-T-C

135290493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627540-A-G

http://identifiers.org/hco/8/GRCh38#135290593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68627629-C-A

135290593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627629-C-G

135290593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627629-C-T

135290636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627670-T-C

135290662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627696-G-A

135290666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627700-G-C

http://identifiers.org/hco/8/GRCh38#135290766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68627779-C-A

135290920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627927-C-T

135291089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628233-A-G

135291288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68628382-G-A

135291297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68628391-T-G

135291353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 68628447-G-A

135291356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628450-A-G

135291359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68628453-C-T

135291382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628488-G-A

135292785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628962-C-G

135292817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628995-C-G

135293020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629177-G-A

http://identifiers.org/hco/8/GRCh38#135293182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68629611-C-A

135293182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629611-C-T

135293236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629660-A-G

135293333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629761-T-C

135293356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629784-C-T

135293359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629855-G-A

135293633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630197-T-G

http://identifiers.org/hco/8/GRCh38#135293638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68630202-C-A

135293638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630202-C-T

135293753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68630319-T-A

135293753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68630319-T-G

135293760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68630320-T-C

http://identifiers.org/hco/8/GRCh38#135293763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68630323-C-A

135293763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68630323-C-T

135293950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630502-G-A

135293950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630502-G-T

135294299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630840-T-A

135294299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630840-T-C

135294309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630850-C-T

135294344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630883-T-G

135294555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631088-C-T

135294581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631118-C-T

http://identifiers.org/hco/8/GRCh38#135294927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68631452-C-A

135295017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631539-G-A

135295190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631693-A-G

135295218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631714-C-G

135295300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631766-G-A

135295300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631766-G-T

135295344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631810-G-A

135295604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632072-C-T

http://identifiers.org/hco/8/GRCh38#135295634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68632102-C-A

135295634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632102-C-T

135295817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632259-C-T

135295880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632324-G-A

135296020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632445-G-A

135296221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632656-T-C

135296316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632751-C-G

135296427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632863-G-T

http://identifiers.org/hco/8/GRCh38#135296526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68632963-A-C

http://identifiers.org/hco/8/GRCh38#135296586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68633025-C-A

http://identifiers.org/hco/8/GRCh38#135296612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#68633052-C-A

135296669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68633110-T-A

135299440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68648045-C-T

135299441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68648046-T-C

135299454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68648058-T-A

135299579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68648160-A-G

135299673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27819
most severe consequence: non coding transcript exon variant
orthologous variants: 68648254-A-T