37341038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78526884-G-A

37341038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78526884-G-C

37341038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78526884-G-T

37341142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78526987-G-A

37341142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78526987-G-T

37341151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78526992-A-G

37341231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78527060-G-A

37341246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527080-G-T

37341248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527082-G-A

37341248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527082-G-C

37341562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527383-G-A

37341620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527420-G-A

37341756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527539-G-C

37342258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527790-G-A

37342348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527848-C-T

37342353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527853-C-T

37342528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527945-T-C

http://identifiers.org/hco/22/GRCh38#37342575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78527996-C-A

37342575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78527996-C-T

37342625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: non coding transcript exon variant
orthologous variants: 78528031-G-A

37342625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: non coding transcript exon variant
orthologous variants: 78528031-G-T

37342804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78528185-G-A

37342804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78528185-G-T

37343053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78528414-A-G

37343176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78528508-C-T

http://identifiers.org/hco/22/GRCh38#37343252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78528587-C-A

37343265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78528600-G-A

37343534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78528920-C-T

37343659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78529082-G-C

37346403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78529617-T-A

37346403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78529617-T-C

37346423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78529637-G-A

37346473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78529696-C-T

37346711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78529949-G-A

37346794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78530072-G-A

37347127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78530382-C-T

37348159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531220-C-T

http://identifiers.org/hco/22/GRCh38#37348261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78531283-A-C

37348275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531292-G-A

37348276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531293-G-T

37348439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531447-T-A

37348823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531682-G-A

37349237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532044-G-T

37349243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532050-G-C

37349357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532160-G-T

37349667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532395-C-T

37349733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532467-C-T

37350933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535197-G-T

http://identifiers.org/hco/22/GRCh38#37350971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78535235-C-A

37350971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535235-C-T

37350979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535242-G-T

37350992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535255-C-T

http://identifiers.org/hco/22/GRCh38#37351236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78535459-A-C

37351505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535709-A-G

http://identifiers.org/hco/22/GRCh38#37351582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78535768-C-A

37360651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545639-T-G

37361224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546545-G-T

37361243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546560-C-T

37361264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546584-G-A

37361300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546619-C-T

http://identifiers.org/hco/22/GRCh38#37361894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78547029-C-A

37361894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78547029-C-T

37362003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78547126-T-A

37362495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78547627-G-C

37367353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551099-G-A

37367376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551122-G-C

37367504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551240-G-A

37367624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551318-G-A

37367825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551422-G-C

37367825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551422-G-T

37367832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551429-A-G

37367897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551483-A-G

37367917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551492-G-A

37367917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551492-G-T

37367954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551527-G-A

37367954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551527-G-T

37368326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78551904-C-T

37368409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78551976-C-T

37368492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78552054-A-G

37368558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78552091-T-C

37368765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78552252-T-C

http://identifiers.org/hco/22/GRCh38#37368845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78552334-C-A

37368845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78552334-C-T

http://identifiers.org/hco/22/GRCh38#37369024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78552452-C-A

http://identifiers.org/hco/22/GRCh38#37369134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78552566-C-A

37369343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78552755-G-T

37369418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78552793-T-C

37369533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78552891-G-T

37369613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78552956-A-G

37369776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553034-G-A

37369776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553034-G-T

http://identifiers.org/hco/22/GRCh38#37369847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78553070-C-A

37369847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553070-C-G

37369847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553070-C-T

http://identifiers.org/hco/22/GRCh38#37369948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78553163-C-A

http://identifiers.org/hco/22/GRCh38#37369960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78553175-A-C

37369960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553175-A-G

37370032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553244-G-A

37370032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553244-G-T

http://identifiers.org/hco/22/GRCh38#37370295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78553478-C-A

37370295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553478-C-T

http://identifiers.org/hco/22/GRCh38#37370342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78553501-C-A

37370342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553501-C-T

37370435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553586-G-A

37370435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553586-G-T

37370452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553598-G-A

37370452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553598-G-T

http://identifiers.org/hco/22/GRCh38#37370474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78553620-C-A

37370495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553637-A-G

37370509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553656-G-T

http://identifiers.org/hco/22/GRCh38#37370552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78553697-C-A

37370552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553697-C-T

37370581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553725-G-A

37370581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553725-G-T

37370700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78553866-T-C

37370992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554127-G-A

37371024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554156-G-A

37371024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554156-G-T

http://identifiers.org/hco/22/GRCh38#37371221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78554340-C-A

37371234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554353-G-A

37371247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554366-G-A

37371247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554366-G-T

37371270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554388-G-T

37371361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554470-T-G

37371543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554621-G-T

http://identifiers.org/hco/22/GRCh38#37371547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78554625-C-A

http://identifiers.org/hco/22/GRCh38#37371566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78554644-C-A

http://identifiers.org/hco/22/GRCh38#37371614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78554696-C-A

37371614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78554696-C-T

http://identifiers.org/hco/22/GRCh38#37371650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78554735-C-A

37371700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78554797-T-C

37372024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78555083-C-T

37372383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78555417-C-T

37372435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78555462-G-A

37372435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78555462-G-T

37372481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78555504-G-A

http://identifiers.org/hco/22/GRCh38#37372533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78555560-C-A

http://identifiers.org/hco/22/GRCh38#37372566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78555578-A-C

37372592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78555604-T-C

37372663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78555675-T-C

37372663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78555675-T-G

37372945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78555924-G-A

37372945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78555924-G-T

37372976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78555955-G-A

37372976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78555955-G-C

37372976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78555955-G-T

37373171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556173-G-A

37373171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556173-G-C

37373171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556173-G-T

37373201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556203-C-T

37373396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556398-G-A

37373396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556398-G-T

37373432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556434-C-T

37373462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556464-G-A

37373462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556464-G-C

37373462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556464-G-T

http://identifiers.org/hco/22/GRCh38#37373582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78556584-C-A

37373582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556584-C-T

37373618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556620-G-A

http://identifiers.org/hco/22/GRCh38#37373828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78556839-A-C

37373855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78556866-G-C

37374023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557034-C-T

37374089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557100-G-A

37374155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557166-G-A

37374344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557355-G-A

37374464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557475-G-A

37374470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557481-A-T

http://identifiers.org/hco/22/GRCh38#37374494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78557505-C-A

37374494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557505-C-T

37374518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557529-G-A

37374518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557529-G-C

37374533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557544-G-A

37374746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557757-G-A

37374847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78557858-G-A

37374847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78557858-G-T

http://identifiers.org/hco/22/GRCh38#37374853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78557864-C-A

37374898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78557909-G-T

http://identifiers.org/hco/22/GRCh38#37375106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78558117-C-A

37375106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78558117-C-T

http://identifiers.org/hco/22/GRCh38#37375301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78558312-A-C

37375415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78558426-G-A

37375436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78558447-G-A

37375511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78558522-C-G

37375511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78558522-C-T

37375560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78558592-A-G

37376004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78558948-G-A

37376004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78558948-G-T

37376109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559056-T-A

37376109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559056-T-C

37376109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559056-T-G

37376111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559058-T-G

37376364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559305-C-T

37377115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559983-C-T

37377164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560029-A-G

37377177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560043-C-G

37377178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560044-T-C

http://identifiers.org/hco/22/GRCh38#37377187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78560053-C-A

37377235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560084-G-T

37377619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560426-G-T

37377631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560438-C-T

37377833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560579-G-A

37378165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560875-G-A

37378172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560882-C-T

37378216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560939-G-A

37378459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561166-C-T

37378802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561485-G-A

37378846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561520-G-A

37379063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561731-G-A

37379063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561731-G-T

37379080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561744-T-G

37379081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561745-G-A

37379121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561776-C-G

37379152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561808-G-A

37379215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561868-C-T

37379254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561901-G-A

37379326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561948-G-A

37379722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78562282-T-C

37379789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78562333-G-A

37380054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78562514-T-C

37380054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78562514-T-G

37380191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78562636-G-A

37380660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563073-C-T

37380963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78563321-C-T

37381183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563527-C-T

37381288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563595-T-C

37381334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563638-C-T

37381383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563685-T-A

37381573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563842-T-A

37381573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563842-T-C

37381573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563842-T-G

37381653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563914-C-T

37381670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563933-C-T

37381702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563969-T-C

37381744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564012-G-A

37381774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564038-G-A

37381774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564038-G-C

http://identifiers.org/hco/22/GRCh38#37382175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78564266-C-A

37383172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564456-C-T

37383245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564493-C-T

37383312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564555-C-T

37383328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564571-G-T

37383471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564701-G-A

http://identifiers.org/hco/22/GRCh38#37383667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78564828-C-A

37384367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565463-C-T

http://identifiers.org/hco/22/GRCh38#37384803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78565670-C-A

37384803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565670-C-T

37384851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78565714-A-G

37384851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78565714-A-T

37384987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78565849-T-C

37385029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78565889-G-T

http://identifiers.org/hco/22/GRCh38#37385328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78566166-C-A

37385328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566166-C-T

37385375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566213-C-T

37385551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566354-G-A

37385591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566384-T-C

37385648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566443-C-T

37385762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566501-C-T

37385973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566700-C-T

37386527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567140-G-T

37386859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567431-G-A

37387091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567654-T-C

37387423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567994-G-A

37387524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568073-C-T

37387651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568173-G-A

37387651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568173-G-T

37387695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568210-C-T

http://identifiers.org/hco/22/GRCh38#37387921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78568404-A-C

37388243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568689-T-C

37388365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568793-G-A

37388562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569011-G-C

37388641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569073-A-T

37388642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569074-G-A

http://identifiers.org/hco/22/GRCh38#37388921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78569274-C-A

37388964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569310-C-T

37389007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569353-T-C

37389113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569479-C-T

37389262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569611-C-T

37389471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569789-G-A

37389632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569933-G-A

37389950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570216-G-C

http://identifiers.org/hco/22/GRCh38#37390206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78570435-A-C

37390241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570470-G-C

37390243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570472-G-A

37390326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570555-A-G

37390379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570579-A-G

37390533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570766-A-G

37390876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571047-G-T

37391003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571171-G-C

37391204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571274-C-G

37391436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571486-C-T

37391523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571555-C-T

37391595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571640-A-T

37391609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571654-C-T

37391707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571729-C-T

37391777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571780-G-A

37391883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571877-G-C

http://identifiers.org/hco/22/GRCh38#37391896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78571890-C-A

37391943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571941-C-T

37391944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571942-G-A

http://identifiers.org/hco/22/GRCh38#37391966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78571972-C-A

http://identifiers.org/hco/22/GRCh38#37391974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78571980-C-A

37392609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572301-C-T

37392610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572302-G-A

37392777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572453-T-C

37392796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572471-G-A

37392796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572471-G-T

37393075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572754-C-T

37393076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572755-C-T

37393097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572776-C-T

37393444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572972-G-T

http://identifiers.org/hco/22/GRCh38#37393522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78573005-C-A

37393667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573148-G-A

37394362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573831-G-A

37394489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573924-C-T

http://identifiers.org/hco/22/GRCh38#37396140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78574741-A-C

37396342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574953-C-T

37396420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575027-C-T

37396611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575154-T-C

http://identifiers.org/hco/22/GRCh38#37396653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78575207-C-A

37396653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575207-C-T

37396777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575500-G-A

http://identifiers.org/hco/22/GRCh38#37396840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78575645-A-C

37396887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575685-G-A

37396887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575685-G-C

37396967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575757-C-T

37397157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575973-C-T

http://identifiers.org/hco/22/GRCh38#37397371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78576096-C-A

37397371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576096-C-T

37397541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576236-G-C

37397564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576251-G-C

37397811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576466-G-A

37398451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577002-C-T

37398464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577015-C-T

37398494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577053-T-G

37398498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577057-G-A

37398785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577481-T-G

http://identifiers.org/hco/22/GRCh38#37398921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78577620-C-A

37398921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577620-C-G

37398996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577698-A-G

37399027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577729-A-G

37399122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577779-C-T

37399236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577857-C-T

37400346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578374-G-A

37400494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578472-A-G

37400521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578493-T-C

http://identifiers.org/hco/22/GRCh38#37400576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78578547-C-A

37400870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578816-T-C

37400880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578826-G-A

37401035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578968-C-T

37401292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579218-A-T

37402085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580036-T-G

http://identifiers.org/hco/22/GRCh38#37402086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78580037-C-A

37403164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582160-G-A

37403244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582216-C-T

37403308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582291-C-G

37403601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582596-G-A

37403601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582596-G-C

37403623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582619-G-A

37403749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582731-G-A

37403749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582731-G-T

http://identifiers.org/hco/22/GRCh38#37403764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78582746-C-A

37404038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582991-G-A

37404527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583420-G-T

37404706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583620-C-T

37404784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583707-G-A

37404805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583728-C-G

37406320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78584531-C-T

37406469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78584638-G-A

37408428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585843-A-T

http://identifiers.org/hco/22/GRCh38#37408549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78585950-C-A

37408549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585950-C-T

http://identifiers.org/hco/22/GRCh38#37408621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78586018-C-A

37408905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586348-T-A

http://identifiers.org/hco/22/GRCh38#37409056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78586470-C-A

37409097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586509-C-T

37409238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586650-C-T

37409239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586651-G-A

37409293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586710-C-T

http://identifiers.org/hco/22/GRCh38#37409304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78586721-C-A

37409510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586833-T-G

37409511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586834-G-A

37409526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586846-G-T

http://identifiers.org/hco/22/GRCh38#37409599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78586919-A-C

37409705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587017-C-T

http://identifiers.org/hco/22/GRCh38#37409831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78587100-C-A

37409834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587103-C-T

37409906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587177-G-C

37410171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587416-G-A

37410213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587457-A-G

37410622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587574-G-T

37411102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587917-G-T

37412575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78589254-G-A

37412781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78589455-T-C

37413392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590159-T-A

37413426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590182-G-A

http://identifiers.org/hco/22/GRCh38#37413664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78590524-C-A

37413974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590807-A-T

37415348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592766-G-A

37415447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592851-G-T

37415498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592881-A-G

http://identifiers.org/hco/22/GRCh38#37415683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78593019-C-A

37415819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593069-A-G

37415823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593073-G-A

37415958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593123-G-A

37416352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593362-G-A

37416419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593431-G-A

37416423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593435-G-A

37416423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593435-G-C

37416423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593435-G-T

37416505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593495-T-C

37416598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593585-C-T

37416794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593878-G-A

37416898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594038-C-T

37417059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594175-C-T

37417165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594282-C-T

37417305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594422-C-T

37417474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594556-C-T

37417580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594636-G-A

37417635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594699-G-A

37417635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594699-G-T

37417713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594770-G-A

37417713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594770-G-T

37417889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78594951-G-T

http://identifiers.org/hco/22/GRCh38#37417923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78594981-C-A

37417923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78594981-C-T

37418617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595941-C-T

http://identifiers.org/hco/22/GRCh38#37418726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78596065-C-A

37418726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596065-C-T

37418843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596156-A-G

37418866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78596163-T-A

37418866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78596163-T-C

37418904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78596204-A-G

37419097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596382-C-T

37419258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596516-T-C

http://identifiers.org/hco/22/GRCh38#37419506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78596651-C-A

37419807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596982-G-A

37420363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78597286-A-T

37420366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78597289-G-A

37420485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78597344-G-A

37420485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78597344-G-T

http://identifiers.org/hco/22/GRCh38#37420634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78597440-C-A

37420634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78597440-C-T

37420680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597484-C-T

http://identifiers.org/hco/22/GRCh38#37420765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78597567-A-C

37420765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597567-A-T

37420824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597601-T-A

37421222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597994-G-A

37421222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597994-G-C

37421237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598012-C-T

37421326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598102-C-T

37421506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598281-A-G

37421632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598342-C-T

37422073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598772-C-T

http://identifiers.org/hco/22/GRCh38#37423228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78599020-A-C

37423234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599026-T-G

37423235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599027-G-T

37423354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599145-A-G

37423502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599290-A-G

37424118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599791-C-T

37424381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599901-G-A

37424535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599984-C-T

37424681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600095-G-A

37424681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600095-G-C

37424681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600095-G-T

37425403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600666-G-A

37425676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600965-C-T

37425814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78601109-G-A

37425967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601271-C-T

37426071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601422-C-T

37426350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601723-G-A

37426350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601723-G-T

37426545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601869-G-A

http://identifiers.org/hco/22/GRCh38#37426566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78601890-A-C

37426566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601890-A-T

http://identifiers.org/hco/22/GRCh38#37426573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78601897-C-A

37426591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601915-G-A

http://identifiers.org/hco/22/GRCh38#37426760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78602048-C-A

37426760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602048-C-T

37426786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602076-T-A

37426786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602076-T-C

37426786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602076-T-G

http://identifiers.org/hco/22/GRCh38#37426804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78602099-C-A

37426822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602131-C-T

37426926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78602235-G-A

37426926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78602235-G-T

37426979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78602289-G-A

37426979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78602289-G-T

37426997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78602304-A-G

37427145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602455-G-A

37427145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602455-G-T

37427146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602456-G-A

http://identifiers.org/hco/22/GRCh38#37427177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78602488-C-A

37427177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602488-C-T

37427178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602489-G-A

http://identifiers.org/hco/22/GRCh38#37427246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78602555-C-A

37427246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602555-C-T

37427272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602578-G-A

37427272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602578-G-C

37427272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602578-G-T

37427337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78602647-G-A

37427343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78602653-G-A

37427343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78602653-G-C

37427343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78602653-G-T