139239350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17725757-G-A

139239357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17725750-G-A

139239393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17725710-G-A

139239543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17723174-A-G

139239544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17723173-G-A

139239544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17723173-G-T

http://identifiers.org/hco/6/GRCh38#139239571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17723149-C-A

139239571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17723149-C-T

http://identifiers.org/hco/6/GRCh38#139239575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17723145-C-A

139239625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17723103-T-C

139239801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17722926-T-C

139239841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17722882-T-C

139239977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17722763-C-T

139240711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720789-G-C

http://identifiers.org/hco/6/GRCh38#139240736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17720764-C-A

139240769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720731-T-C

139240924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720576-G-T

139240991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720534-T-C

139240991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720534-T-G

139240995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720530-T-C

139241020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720504-C-G

139241057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720466-G-A

139241057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720466-G-T

139241157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720362-T-C

139241171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720347-T-C

139241191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720329-A-G

139241303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720211-G-C

139241377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720140-A-G

139241383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17720133-T-G

http://identifiers.org/hco/6/GRCh38#139241522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17720019-C-A

139241579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719959-T-A

139241579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719959-T-C

139241600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719938-G-A

139241618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719910-G-A

139241618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719910-G-T

139241638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719893-C-T

139241659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719883-T-A

139241701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719838-G-T

139241707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719832-G-A

139241707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719832-G-T

139241880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719770-A-G

139241900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719750-G-T

139241934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719721-G-T

139242163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719532-A-T

139242169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719526-T-G

139242329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719397-A-G

http://identifiers.org/hco/6/GRCh38#139242372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17719355-C-A

139242407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719325-T-A

139242407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719325-T-C

139242407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719325-T-G

139242519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719233-G-A

139242519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17719233-G-T

139242532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17719220-G-A

139242532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17719220-G-C

139242532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17719220-G-T

139242537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17719215-C-G

139242537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17719215-C-T

139242550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17719202-G-A

139242590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17719168-A-G

139242625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17719136-C-T

139242641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17719120-G-A

139242642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17719119-C-T

139242712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17719049-T-A

139242712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17719049-T-C

139242712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17719049-T-G

139242849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718918-T-A

139242849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718918-T-C

139242862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17718905-A-T

139242864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718903-G-A

http://identifiers.org/hco/6/GRCh38#139242885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#17718882-C-A

139242885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718882-C-T

139242900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718867-G-A

139242904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17718863-T-C

139242959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718799-G-A

139242959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718799-G-T

139242973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17718785-G-A

139242973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17718785-G-C

139243007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718751-G-A

139243007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718751-G-T

139243158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17718600-C-T

139243377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17718374-C-T

139243429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17718335-A-G

139243552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17718253-C-T

139243572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17718233-G-A

139243587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17718218-T-G

139243886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717911-C-T

139244217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717594-T-C

139244333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717494-A-G

139244400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717433-G-A

http://identifiers.org/hco/6/GRCh38#139244495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17717339-C-A

139244495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717339-C-T

139244500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717334-A-G

139244611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 17717251-A-G

139244611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 17717251-A-T

139244626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 17717236-C-G

139244626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 17717236-C-T

139244751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717119-T-A

139244784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717087-T-C

139244785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717086-G-A

139244785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717086-G-T

139244807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17717064-A-G

139245062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716805-G-A

139245386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716517-G-A

139245444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716470-A-T

139245824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716232-C-T

139245849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716204-T-C

139245885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716163-T-G

139245985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716087-G-A

139245985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716087-G-C

139245985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17716087-G-T

139246559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17715237-T-C

139246560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17715236-G-A

139247715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17714841-A-T

139247765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17714794-G-T

139248037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17714484-T-A

139248037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17714484-T-C

139251536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17712495-T-C

139251725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17712208-T-A

139251988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17711877-A-T

139252018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17711847-T-G

139252276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17711400-A-T

139252310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17711367-G-A

139253729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710807-G-A

139253856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710692-A-G

139253859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710689-G-A

139253859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710689-G-T

139253935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710618-T-A

139253959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710570-C-G

139253959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710570-C-T

139254105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710410-A-T

139254192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17710327-A-G

http://identifiers.org/hco/6/GRCh38#139254462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17709826-A-C

139255238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709398-A-G

139255238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709398-A-T

139255240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709396-G-A

139255260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709376-G-A

139255273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709364-G-T

http://identifiers.org/hco/6/GRCh38#139255278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17709359-C-A

139255278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709359-C-G

139255278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709359-C-T

http://identifiers.org/hco/6/GRCh38#139255317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17709320-C-A

139255344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709296-G-T

139255349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709291-T-C

139255352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709288-C-T

http://identifiers.org/hco/6/GRCh38#139255356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17709284-C-A

139255356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709284-C-T

139255444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17709214-A-G

139255474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17709192-G-A

139255474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17709192-G-T

139255660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17709002-G-C

http://identifiers.org/hco/6/GRCh38#139255742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17708924-C-A

139255742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708924-C-T

139255743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708923-T-A

139255743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708923-T-G

139255748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708918-T-A

139255756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708897-T-C

139256228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708742-A-T

139256262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708713-G-A

139256264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708711-C-G

139256270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708705-T-G

139257968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708023-T-A

139257993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17708001-C-T

139258022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17707968-T-G

139258110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17707910-C-T

139259257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17707183-G-A

139259276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17707164-A-G

139259353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17707094-G-T

139259392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17707061-C-T

139259735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17706363-C-T

139259860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17706238-T-C

139260452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17705970-G-T

139260469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17705954-G-T

139260604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17705838-G-A

http://identifiers.org/hco/6/GRCh38#139260763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17705689-A-C

139260959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17705450-G-C

139261003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17705318-G-A

139261057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17705258-A-T

139261077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17705241-G-A

139261466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17704745-T-C

139262419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703893-T-C

139262450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703862-A-G

139262450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703862-A-T

139262460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703852-A-G

139262467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703846-A-G

139262494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703820-T-C

139262535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703778-T-A

139262586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17703725-C-T

139262598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17703713-T-G

139262810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703496-C-T

139262996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703346-T-A

139263073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17703269-C-T

139263320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17702916-G-A

139263479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17702683-A-G

139263551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17702599-A-G

139263570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17702585-T-C

139263986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17702170-G-A

139264117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17702062-G-A

139264392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17701810-C-G

139264504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17701739-A-G

139264504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17701739-A-T

139265069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17701395-C-T

139265171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17701308-T-A

139265372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17701110-A-G

139265503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17701022-A-G

139265517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17701008-G-A

139265600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700962-T-A

139265983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700632-T-C

139265984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700631-G-A

139266002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700613-C-T

139266069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700551-A-T

139266160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700389-A-G

139266160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700389-A-T

139266204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700341-T-C

139266226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700335-G-A

139266349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17700066-T-C

139266383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17699968-G-A

139266555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17699740-A-G

http://identifiers.org/hco/6/GRCh38#139266619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17699634-C-A

139266619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17699634-C-T

139266651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17699602-A-G

139266790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17699474-A-G

139266808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17699383-G-A

139266853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17699184-G-C

139267058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17699011-T-C

139267207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17698859-A-T

http://identifiers.org/hco/6/GRCh38#139267328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17698737-A-C

139267334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17698732-T-A

139267364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17698702-T-C

139267405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17698665-T-C

139267444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17698627-G-C

139267456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17698615-T-C

139267466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17698605-G-T

http://identifiers.org/hco/6/GRCh38#139267800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17698221-A-C

139267800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17698221-A-G

http://identifiers.org/hco/6/GRCh38#139269243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17697253-C-A

139269305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17697207-T-A

139269318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17697194-T-C

139269318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17697194-T-G

139269344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17697168-A-G

139269418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17697114-C-T

139269431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17697101-G-A

139269470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17697059-G-A

139269786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17696044-T-C

139269839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17696003-C-T

139269855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17695986-G-A

139269953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17691871-T-C

139270336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17691264-A-T

http://identifiers.org/hco/6/GRCh38#139270351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17691249-C-A

139270351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17691249-C-T

http://identifiers.org/hco/6/GRCh38#139270421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17691182-A-C

139270435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17691168-T-C

139270444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17691159-A-G

139270445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17691158-T-C

139270519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17691082-G-A

139270634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 17690969-C-T

139270635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690968-A-G

139270647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690956-A-G

http://identifiers.org/hco/6/GRCh38#139270668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17690935-A-C

139270668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690935-A-G

139270668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690935-A-T

139270702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690900-A-G

139270724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690877-G-A

139270724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690877-G-T

139270726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690875-A-G

http://identifiers.org/hco/6/GRCh38#139270758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17690843-A-C

139270758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690843-A-G

139270899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690685-A-G

139270971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690605-T-A

139270971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690605-T-G

http://identifiers.org/hco/6/GRCh38#139271175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17690389-A-C

139271235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690319-G-C

139271241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690313-G-T

http://identifiers.org/hco/6/GRCh38#139271255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17690299-C-A

139271330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690218-T-G

http://identifiers.org/hco/6/GRCh38#139271473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17690144-C-A

139271481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17690136-G-T

139271482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17690135-G-C

139271579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17690047-T-C

139271656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 17689963-C-T

http://identifiers.org/hco/6/GRCh38#139271714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17689906-C-A

139271714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689906-C-G

139271714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689906-C-T

139271753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689867-T-A

139271753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689867-T-C

139271761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689859-A-G

http://identifiers.org/hco/6/GRCh38#139271762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17689858-C-A

139271762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689858-C-T

139271772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689848-G-A

139271784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689836-G-A

139271803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689817-A-G

http://identifiers.org/hco/6/GRCh38#139271840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17689780-C-A

139271853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689767-A-G

139271853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17689767-A-T

http://identifiers.org/hco/6/GRCh38#139271857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17689763-A-C

139271857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 17689763-A-G

139271857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 17689763-A-T

139271864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17689756-T-C

139271877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17689744-A-G

139271878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17689743-A-G

http://identifiers.org/hco/6/GRCh38#139271879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17689742-C-A

139271879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17689742-C-T

139272005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17689606-C-T

139272468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17689468-T-C

139272662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17689279-C-T

139273135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17686648-G-A

139273353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17686475-T-C

139273424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17686405-G-A

139274040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685632-G-C

139274047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685617-A-T

139274260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685418-T-C

139274452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685239-G-A

139274654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685110-C-G

http://identifiers.org/hco/6/GRCh38#139274658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17685106-C-A

139274658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685106-C-G

139274658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685106-C-T

http://identifiers.org/hco/6/GRCh38#139274659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17685105-C-A

139274659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685105-C-G

139274696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685069-T-C

139274748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17685029-T-C

139274796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17684980-G-A

139274856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17684919-A-G

http://identifiers.org/hco/6/GRCh38#139274956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17684814-A-C

139275072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17684728-A-G

139275670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683707-A-G

139275676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683701-G-T

139275756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683653-G-C

139275783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683625-C-G

139275783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683625-C-T

139275819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683598-C-G

139276719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683331-T-A

139276728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683322-T-C

139276741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683302-T-G

139276755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683286-G-T

139276770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683268-A-G

139276778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683261-G-T

139276779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683260-G-A

139276779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17683260-G-T

139276805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682627-A-G

139276935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682497-G-A

139276935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682497-G-C

139276935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682497-G-T

http://identifiers.org/hco/6/GRCh38#139276946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17682480-A-C

139276946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682480-A-G

139276950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682476-A-T

139277057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682370-T-C

139277057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682370-T-G

139277064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682363-A-G

http://identifiers.org/hco/6/GRCh38#139277086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17682342-C-A

139277118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17682324-G-T

http://identifiers.org/hco/6/GRCh38#139277151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17682291-C-A

http://identifiers.org/hco/6/GRCh38#139277170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17682272-C-A

139277170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17682272-C-G

139277170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17682272-C-T

139277187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17682255-T-C

139277224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682223-T-C

139277224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682223-T-G

139277243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682203-T-G

139277336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682109-G-A

139277400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682039-A-G

139277400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682039-A-T

139277443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17682005-T-C

139277451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17681997-T-G

139277522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17681961-T-C

139277579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17681905-G-C

139277625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17681858-A-G

139277753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17681587-T-C

139277772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17681568-T-C

139277790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17681550-A-G

http://identifiers.org/hco/6/GRCh38#139277881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17681451-A-C

139277991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17681318-G-A

139278479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17680841-G-A

139278479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17680841-G-T

139278485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17680835-C-T

139279106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17680537-A-T

139279220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17680432-T-G

139279516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17680213-G-A

139279630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17680128-A-G

http://identifiers.org/hco/6/GRCh38#139279657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17680105-A-C

139279657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17680105-A-G

139279890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17679873-C-G

139280325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17679703-C-T

139280829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17679416-T-C

139280887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17679365-G-A

139281028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17679276-C-T

139281332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17679026-G-T

139281467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17678909-T-C

139281927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17678773-G-A

139284828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17677864-T-C

139284968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17677730-G-A

139285679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17677104-A-G

139287405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17677084-G-T

139287525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17676968-T-A

139287703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17676821-C-G

139287718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17676804-A-G

139287730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17676792-A-G

139287741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17676780-A-G

139288027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17675949-T-C

139288045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17675932-G-A

139288045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17675932-G-T

http://identifiers.org/hco/6/GRCh38#139288343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17675651-C-A

139288432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17675322-G-T

http://identifiers.org/hco/6/GRCh38#139288438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17675316-C-A

139288438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17675316-C-T

139288537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17675218-A-G

139288538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17675217-G-T

http://identifiers.org/hco/6/GRCh38#139288643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17675112-C-A

139288643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17675112-C-G

139288643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17675112-C-T

139288657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17675098-G-A

139288851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17674892-G-A

139288851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17674892-G-T

http://identifiers.org/hco/6/GRCh38#139288874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17674872-A-C

139288933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674814-G-A

http://identifiers.org/hco/6/GRCh38#139289003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#17674760-A-C

139289003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674760-A-T

139289005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674758-T-G

139289023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674740-T-A

139289023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674740-T-C

139289023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674740-T-G

139289029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674734-G-A

139289029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674734-G-C

139289029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674734-G-T

139289048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674719-T-A

139289048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674719-T-C

139289048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674719-T-G

139289658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674608-G-A

139289862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17674440-T-G

139290459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17673825-A-G

139290625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17673507-T-A

139290625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17673507-T-C

139291005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17673131-C-T

139291340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17672808-A-G

139291595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17672493-G-A

139291684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17672400-T-C

http://identifiers.org/hco/6/GRCh38#139291787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#17672295-C-A

139291874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17672216-A-G

139291874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17672216-A-T

139291896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17672192-T-C

139291971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17672107-A-G

139292151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17671967-G-T

http://identifiers.org/hco/6/GRCh38#139292245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#17671875-A-C

139292760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21617
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17671406-A-T