116881485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58958997-G-C

116881490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959002-T-C

116881520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 58959053-A-G

116881602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 58959123-C-T

116881642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 58959163-A-G

http://identifiers.org/hco/10/GRCh38#116881694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959210-C-A

116881694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959210-C-T

http://identifiers.org/hco/10/GRCh38#116881733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959245-C-A

116881733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959245-C-T

116881810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959332-T-C

http://identifiers.org/hco/10/GRCh38#116881897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959404-C-A

116881897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959404-C-T

http://identifiers.org/hco/10/GRCh38#116881940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959450-A-C

116881940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959450-A-G

116881958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959470-T-A

http://identifiers.org/hco/10/GRCh38#116881962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959474-C-A

116881962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959474-C-T

http://identifiers.org/hco/10/GRCh38#116882169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959704-C-A

http://identifiers.org/hco/10/GRCh38#116882338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959860-C-A

http://identifiers.org/hco/10/GRCh38#116882367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58959889-C-A

116882432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58959925-A-G

116882618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960086-G-T

116882968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960399-A-G

http://identifiers.org/hco/10/GRCh38#116882995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960411-C-A

116882995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960411-C-T

116883170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960536-T-C

116883191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960557-C-T

116883193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960559-A-G

116883263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960639-C-T

116883435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960694-T-A

http://identifiers.org/hco/10/GRCh38#116883553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960728-C-A

116883651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960817-T-C

116883651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960817-T-G

http://identifiers.org/hco/10/GRCh38#116883673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960833-C-A

116883673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960833-C-T

http://identifiers.org/hco/10/GRCh38#116883674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960834-C-A

116883674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960834-C-T

116883682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58960838-T-C

http://identifiers.org/hco/10/GRCh38#116883888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58960987-C-A

http://identifiers.org/hco/10/GRCh38#116883970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961042-C-A

116884015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961085-G-A

http://identifiers.org/hco/10/GRCh38#116884185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961205-C-A

http://identifiers.org/hco/10/GRCh38#116884343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961305-C-A

116884343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961305-C-T

http://identifiers.org/hco/10/GRCh38#116884347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961309-C-A

116884347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961309-C-T

116884597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961572-G-T

116884604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961585-T-G

116884646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961626-G-A

116884646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58961626-G-T

116884830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58961819-G-C

http://identifiers.org/hco/10/GRCh38#116884898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961887-C-A

http://identifiers.org/hco/10/GRCh38#116884964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58961956-C-A

116884964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58961956-C-T

116885029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962019-A-T

116885179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962168-G-T

http://identifiers.org/hco/10/GRCh38#116885193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58962182-A-C

116885193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962182-A-G

116885285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962274-T-C

116885337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962326-C-T

116885689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962694-G-T

116885857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962845-T-C

http://identifiers.org/hco/10/GRCh38#116885862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58962850-C-A

116885876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962864-T-C

116885878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962866-C-G

116885878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962866-C-T

116885884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962872-T-C

116885891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962879-G-T

116885904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962890-G-A

116885904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58962890-G-T

http://identifiers.org/hco/10/GRCh38#116886122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58963221-C-A

116886122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58963221-C-T

116886363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58963437-G-A

116886363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58963437-G-C

116886476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58963550-A-G

116886585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58963658-G-A

116886585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58963658-G-C

116886622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58963696-T-C

116887022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58964101-G-A

116887071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58964160-G-C

116887090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58964181-G-A

116887305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58964392-G-C

116887354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58964498-A-G

116887650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58964781-T-C

http://identifiers.org/hco/10/GRCh38#116888536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58965396-C-A

http://identifiers.org/hco/10/GRCh38#116888583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#58965439-C-A

116888585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58965442-A-T

116888713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58965585-C-G

116888717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58965589-T-A

116888734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58965606-C-G

116888752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58965620-G-A

116888854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58965714-T-G

116888863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58965723-C-T

116890125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58967089-A-G

116890262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58967219-C-T

116890296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58967273-T-C

116890359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58967338-T-C

116890390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58967366-G-C

http://identifiers.org/hco/10/GRCh38#116890792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58967706-C-A

116890838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58967749-G-C

116890858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58967771-A-G

http://identifiers.org/hco/10/GRCh38#116891724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58968657-A-C

116891911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58968799-G-T

116892095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58968927-G-A

116892095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58968927-G-C

116892281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58969071-C-G

116892409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58969158-T-C

116892638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58969399-T-C

116892642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58969403-T-C

116892703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58969473-G-A

116893170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58969959-G-T

http://identifiers.org/hco/10/GRCh38#116893541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58970337-C-A

116893541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58970337-C-T

116893575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58970406-T-C

116893763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58970613-A-G

116893774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58970628-T-C

116894040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58970848-T-C

116894256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58971069-C-T

116894298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58971116-G-A

116894298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58971116-G-T

116894422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58971256-T-C

http://identifiers.org/hco/10/GRCh38#116895370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58972379-A-C

116895852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58972835-C-G

116895852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58972835-C-T

116895952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58972948-C-T

116896193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58973175-A-G

116896201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58973183-C-T

116896702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58973587-C-T

116896768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58973650-G-C

116896791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58973668-T-C

http://identifiers.org/hco/10/GRCh38#116900194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58977137-C-A

116900194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58977137-C-T

116900304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58977247-T-C

116900578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58977525-A-T

116900913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58977836-T-A

116900913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58977836-T-C

116901002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58977929-T-C

116901019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58977945-G-A

116901196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978122-C-T

116901218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978144-A-G

116901240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978164-T-C

116901477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978364-G-C

116901626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978495-G-A

116901662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978527-G-A

116901662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978527-G-C

116901662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978527-G-T

http://identifiers.org/hco/10/GRCh38#116901670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58978532-C-A

http://identifiers.org/hco/10/GRCh38#116901721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58978577-C-A

116901721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978577-C-G

116901721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978577-C-T

116901756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978612-G-A

116901756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978612-G-T

116902091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978945-G-A

116902091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978945-G-T

116902105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978967-G-A

116902105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58978967-G-C

116902225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58979083-G-A

116902242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58979100-G-A

116902263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58979121-T-C

116902559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58979424-G-C

116902630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58979495-G-A

116902630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58979495-G-T

116903540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58980262-G-T

http://identifiers.org/hco/10/GRCh38#116903542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58980264-C-A

116903542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58980264-C-T

116903652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58980367-A-T

116903660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58980375-G-C

116903844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58980563-C-T

116903955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58980657-G-A

116904614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58981260-A-G

116904656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58981296-G-C

http://identifiers.org/hco/10/GRCh38#116904712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58981343-A-C

116904712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58981343-A-G

116904727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58981358-T-G

http://identifiers.org/hco/10/GRCh38#116904787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58981402-C-A

http://identifiers.org/hco/10/GRCh38#116906127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58982615-A-C

116906160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58982648-T-A

116906582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58983405-T-C

116906913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58983729-G-C

116907176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58983964-G-A

116907210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58983999-C-T

116907253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984035-T-C

116907253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984035-T-G

116907490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984254-G-A

116907518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984277-C-T

116907586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984339-C-T

116907601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984350-C-T

116907715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984454-G-A

116907768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984504-A-T

116907836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984544-G-A

116907836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984544-G-C

116907918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984601-A-G

116907918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58984601-A-T

116908428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58985031-T-C

116908540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58985143-A-G

116908545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58985148-T-C

116908995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58985538-A-G

116909226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58985801-T-C

116909409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58985939-T-C

116909417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58985947-T-C

116910148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58986598-G-A

116910771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58987235-A-G

116911252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58987688-G-A

116911567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58988110-G-A

116911568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58988111-T-C

116911590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58988133-A-T

116911624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58988153-T-C

116911666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58988205-C-G

116911666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58988205-C-T

http://identifiers.org/hco/10/GRCh38#116911888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58988425-A-C

116912246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58989296-C-T

116913683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58990512-T-C

http://identifiers.org/hco/10/GRCh38#116913706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58990533-C-A

http://identifiers.org/hco/10/GRCh38#116914080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58990790-C-A

116914538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58991223-G-A

http://identifiers.org/hco/10/GRCh38#116914661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58991316-A-C

116914687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58991355-A-G

116914714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58991382-G-T

116915103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58991690-T-C

http://identifiers.org/hco/10/GRCh38#116915345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58992212-C-A

116915349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58992216-G-T

116915577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58992465-T-G

116915679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58992580-T-A

116916029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58993186-G-A

116916055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58993212-C-T

116916281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58993783-G-A

116916375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58993871-C-T

116916445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58993924-C-G

116916494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58993956-T-C

116916562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58994014-C-T

116916658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58994091-T-C

116916792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58994212-G-A

116916806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58994226-A-G

116917593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58995127-T-C

116918012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58995551-A-G

116918385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58996082-G-C

116918390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58996087-T-G

116918426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58996121-C-T

116918440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58996122-C-T

116920487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58997006-C-G

116920508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58997030-T-C

116920669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58997170-A-G

116920701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58997202-C-T

116920748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58997247-A-G

116920748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58997247-A-T

116920818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58997314-T-C

116920961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58997438-G-A

116921406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58998163-C-G

116921406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58998163-C-T

116921407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58998164-A-G

116921424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58998187-T-C

http://identifiers.org/hco/10/GRCh38#116921545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58998308-A-C

http://identifiers.org/hco/10/GRCh38#116921591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#58998376-C-A

116921591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58998376-C-G

116922384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58999324-A-T

116922633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58999547-T-C

116923918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59000306-T-C

116924352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59000725-A-G

116925231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59001085-A-T

116925260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59001110-G-A

116925369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59001211-T-C

116925661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59001635-T-A

116925694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59001667-T-C

http://identifiers.org/hco/10/GRCh38#116925993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59001945-C-A

116925993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59001945-C-G

116926099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59002041-C-T

http://identifiers.org/hco/10/GRCh38#116926118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59002060-C-A

116926118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59002060-C-T

116926156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59002103-G-A

116926156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59002103-G-C

116926471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59002407-G-A

116927204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59003092-C-G

116927204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59003092-C-T

116927229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59003116-A-G

116927887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59004054-A-G

116927887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59004054-A-T

http://identifiers.org/hco/10/GRCh38#116927933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59004113-A-C

http://identifiers.org/hco/10/GRCh38#116928004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59004175-C-A

116928004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59004175-C-T

116928025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59004196-G-A

116929047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59005859-T-C

116929222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59006029-T-C

116929706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59006527-A-G

116929732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007145-G-T

116929739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007153-T-C

116929790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007194-T-G

http://identifiers.org/hco/10/GRCh38#116929842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59007230-C-A

116929934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59007322-T-C

116929947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59007335-T-C

http://identifiers.org/hco/10/GRCh38#116930041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59007423-C-A

116930042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007424-A-G

116930042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007424-A-T

http://identifiers.org/hco/10/GRCh38#116930088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59007468-C-A

116930088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007468-C-T

116930107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007510-G-A

116930107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007510-G-T

http://identifiers.org/hco/10/GRCh38#116930124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59007527-C-A

http://identifiers.org/hco/10/GRCh38#116930133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59007536-A-C

116930133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59007536-A-G

116932914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59009110-C-T

116933066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59009326-C-T

116940418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59010560-T-C

116940418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59010560-T-G

http://identifiers.org/hco/10/GRCh38#116940667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59010809-A-C

116940667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59010809-A-T

http://identifiers.org/hco/10/GRCh38#116940688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59010824-A-C

116940754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59010882-T-A

116940923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59011031-T-G

116940931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59011039-T-G

116941038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59011131-G-A

116941739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59011775-G-C

116943032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014483-T-C

116943036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014487-C-G

116943050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014500-G-C

116943099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014557-T-C

116943209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014644-A-G

116943374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014808-T-A

116943374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014808-T-C

116943395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014828-A-G

116943451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014866-A-T

116943488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014899-T-C

116943511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014922-G-A

116943529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014942-A-G

116943553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59014966-C-G

116943720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59015187-A-T

http://identifiers.org/hco/10/GRCh38#116943827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59015287-C-A

116943827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59015287-C-T

116943873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59015335-T-C

116944014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59015484-G-A

116944225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59015685-T-G

116944550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59016048-C-G

116944566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59016064-A-T

116944898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59016561-A-G

116944898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59016561-A-T

116944914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59016577-A-G

116944917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59016580-T-C

116944979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59016642-A-T

116945118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59016751-A-G

http://identifiers.org/hco/10/GRCh38#116945127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59016760-C-A

116945127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59016760-C-T

116945216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59016842-T-C

http://identifiers.org/hco/10/GRCh38#116945375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59016966-A-C

116947255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59017595-T-C

http://identifiers.org/hco/10/GRCh38#116947624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59017958-A-C

http://identifiers.org/hco/10/GRCh38#116947714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59018049-A-C

116948776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020486-G-A

116948776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020486-G-C

116948776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020486-G-T

116948793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020504-T-A

116948793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020504-T-C

116948793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020504-T-G

http://identifiers.org/hco/10/GRCh38#116948834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59020533-C-A

116948834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020533-C-T

116948835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020534-A-T

http://identifiers.org/hco/10/GRCh38#116948876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59020575-C-A

116948876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020575-C-T

116948896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020585-A-G

116948953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59020642-A-G

116949080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59020759-T-C

116951007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59022410-G-A

116951047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59022443-G-C

116951927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59023494-G-A

116951927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59023494-G-C

116951927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59023494-G-T

116952020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59023587-G-A

116952020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59023587-G-T

116952022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59023589-A-G

116952033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59023604-T-A

116952033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59023604-T-C

116952033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59023604-T-G

116952078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59024758-A-T

116952194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59024868-T-C

116952317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59024984-T-C

116952931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59025492-T-C

116953171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59025696-A-G

116953391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59026032-T-A

116953489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59026138-T-G

116953570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59026227-T-C

116953679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59026364-G-T

http://identifiers.org/hco/10/GRCh38#116953706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59026393-C-A

116953957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59026580-C-T

116953975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59026598-T-C

http://identifiers.org/hco/10/GRCh38#116954027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59026635-A-C

116954027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59026635-A-T

116954400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59027026-C-G

116954457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59027082-G-C

116958346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59028148-T-C

http://identifiers.org/hco/10/GRCh38#116958378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59028180-C-A

116958438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59028240-A-G

116958610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59028491-C-T

116958820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59028863-T-C

116958821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59028864-A-G

116958921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59028969-T-C

116959011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59029023-C-T

http://identifiers.org/hco/10/GRCh38#116959231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59029211-A-C

116959728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59029696-A-T

116960157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59030315-A-G

116960461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59030738-T-C

116962743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59033265-A-G

116962803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59033350-T-G

116963009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59033552-T-G

116964062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59035263-C-T

116964168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59035328-G-A

http://identifiers.org/hco/10/GRCh38#116965188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59036230-C-A

116965188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59036230-C-T

116965842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59036451-G-A

http://identifiers.org/hco/10/GRCh38#116966702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59037260-C-A

116967123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59037654-G-A

116967145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59037675-T-G

116967814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59038385-G-C

116967910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59038474-G-A

http://identifiers.org/hco/10/GRCh38#116968485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59039108-C-A

116968510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039133-G-A

116968510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039133-G-C

116968510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039133-G-T

116968519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039147-G-T

116968541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039169-T-C

116968554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039182-T-G

http://identifiers.org/hco/10/GRCh38#116968569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59039197-C-A

116968569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039197-C-G

http://identifiers.org/hco/10/GRCh38#116968698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59039312-C-A

116968724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039345-G-C

116968728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039349-T-C

116968766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039385-G-T

116968844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59039708-A-T

http://identifiers.org/hco/10/GRCh38#116968984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59039974-C-A

116971402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59040550-T-G

116971502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59040611-C-T

116971503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59040612-T-C

116971576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59040684-C-T

116971655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59040764-A-G

116971874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59040971-G-A

116971875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59040972-G-T

116971907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59040999-A-G

http://identifiers.org/hco/10/GRCh38#116971997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59041093-C-A

116972529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59041614-A-T

116972558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59041642-G-A

116972558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59041642-G-C

116972739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59041819-A-G

116972786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59041866-T-C

http://identifiers.org/hco/10/GRCh38#116973029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59042097-A-C

116974119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59042465-C-T

116974391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59042751-C-T

116974398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59042758-G-A

116974398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59042758-G-C

116974407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59042769-A-G

116974407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59042769-A-T

116974748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59043131-G-A

116974852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59043267-C-T

116975149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59043577-T-C

116975662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59044859-T-A

116975662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59044859-T-C

116975865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59045239-A-G

116975890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59045258-A-G

116976006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59045689-C-T

116976061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59045745-C-T

116976238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59045934-T-C

116976394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59046052-T-C

116976408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59046075-A-G

116976693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59046359-T-C

116976758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59046424-A-G

116977185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59046829-A-G

116977225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59046888-T-G

116977594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59047385-A-G

http://identifiers.org/hco/10/GRCh38#116978099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59047789-C-A

116978198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59047889-T-C

116978236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59047928-C-T

116978558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59048321-G-T

116978635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59048461-T-C

116978662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59048487-T-C

116979058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59048878-G-C

116979148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59048963-A-T

http://identifiers.org/hco/10/GRCh38#116979152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59048967-C-A

116979152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59048967-C-T

116979181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59048993-G-C

116979181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59048993-G-T

116979213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049025-T-G

116979222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049034-G-A

116979222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049034-G-C

116979222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049034-G-T

116979306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 59049113-T-C

116979369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049181-G-A

116979389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049201-A-G

116979427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049237-G-T

http://identifiers.org/hco/10/GRCh38#116979442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59049248-C-A

116979744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049353-G-T

116979782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049386-T-G

116979925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049520-C-T

116980154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59049702-G-C

http://identifiers.org/hco/10/GRCh38#116980606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59049880-C-A

116980756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59050156-T-C

116981534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59050508-C-T

116981591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59050564-T-C

116981658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59050631-A-G

116982286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59051536-A-G

http://identifiers.org/hco/10/GRCh38#116982334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59051604-A-C

116982388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59051729-G-A

116982975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59052188-G-A

116982975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59052188-G-C

http://identifiers.org/hco/10/GRCh38#116982978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59052191-C-A

http://identifiers.org/hco/10/GRCh38#116983164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59052351-C-A

116983614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59052747-G-A

116983614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59052747-G-C

116983917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59052927-T-C

http://identifiers.org/hco/10/GRCh38#116984261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59053265-A-C

116984373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053340-T-C

116984383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053350-A-G

116984533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053511-A-G

116984534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053512-T-A

http://identifiers.org/hco/10/GRCh38#116984554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59053516-C-A

116984556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053518-A-G

116984686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59053624-G-A

116984735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053670-T-C

116984819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053746-T-C

116984919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053793-G-A

116984919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053793-G-C

116984931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59053805-A-T

116985140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59054178-C-T

116985182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59054222-A-G

116985285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59054338-T-C

116985286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59054339-C-T

http://identifiers.org/hco/10/GRCh38#116985289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59054342-C-A

116986180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59055185-T-A

116986244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59055241-A-G

http://identifiers.org/hco/10/GRCh38#116986303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59055298-A-C

116986981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59055814-C-G

116987013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59055843-C-T

116987196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59055970-A-G

116987249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59056022-C-G

116987266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59056039-A-T

116987383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59056142-C-T

http://identifiers.org/hco/10/GRCh38#116989154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59056900-A-C

117000235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59059871-G-A

117000383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59060029-T-C

117000530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59060338-C-T

117000656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59060542-A-G

117000662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59060548-G-A

117000932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59060826-G-T

117001506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59061408-A-G

117002097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59061686-T-C

http://identifiers.org/hco/10/GRCh38#117002148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59061737-C-A

117002251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59061835-G-A

117002346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59061928-G-A

117003053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59062494-C-G

117003073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59062514-T-G

117003598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59062979-A-G

117003681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063029-C-T

117003731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063068-G-C

117004223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063195-C-T

117004394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59063327-G-A

http://identifiers.org/hco/10/GRCh38#117004416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59063342-C-A

117004416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063342-C-T

117004417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063343-G-A

117004920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063794-A-G

117004933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063809-G-A

117004933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063809-G-C

117004933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063809-G-T

117004934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063810-G-A

117004934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59063810-G-T

http://identifiers.org/hco/10/GRCh38#117004957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59063827-C-A

117004957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59063827-C-G

117004957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59063827-C-T

117004975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59063843-G-A

117004975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59063843-G-C

117004975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, undefined
orthologous variants: 59063843-G-T

http://identifiers.org/hco/10/GRCh38#117005157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59064021-A-C

117005179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59064048-C-T

http://identifiers.org/hco/10/GRCh38#117005359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59064217-C-A

117005359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59064217-C-T

117005370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59064228-C-T

117005429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59064280-G-A

http://identifiers.org/hco/10/GRCh38#117005518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59064321-A-C

117005615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064418-G-A

117005615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064418-G-C

117005615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064418-G-T

117005629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064432-G-A

117005629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064432-G-T

117005717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064499-G-A

117005717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064499-G-T

117005725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064507-G-T

117005742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59064525-G-A

117006918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59065543-A-G

117007043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59065654-A-G

117008382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59067279-G-A

117008606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59067507-G-A

117008606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59067507-G-C

117008976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59067927-G-A

117008984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59067935-A-G

117014492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59073475-A-G

117014691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59073698-T-C

117014710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59073715-A-G

117014818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59073866-C-T

117014820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59073868-T-C

117014925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59074121-C-G

117014925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59074121-C-T

117015050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59074239-C-T

117015731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59074725-C-T

117015884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59074867-G-A

117045231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59080216-A-G

117045232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59080217-C-T

117045239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59080224-G-C

117045339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59080352-T-C

117048070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59086159-A-G

117048091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59086180-A-G

http://identifiers.org/hco/10/GRCh38#117048334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59086423-C-A

117048334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59086423-C-G

117048563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59086655-G-A

117048563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59086655-G-T

117048846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59086937-G-A

117049307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59088680-G-A

http://identifiers.org/hco/10/GRCh38#117049373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59088727-C-A

http://identifiers.org/hco/10/GRCh38#117049563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59088897-C-A

117060606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59102406-T-C

http://identifiers.org/hco/10/GRCh38#117060639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59102373-A-C

117060727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59102287-T-C

117060763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59102251-G-C

117060787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59102232-A-G

117060959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59102076-T-C

117060960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59102075-T-G

117061099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59101945-G-C

117069974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59107648-T-G

http://identifiers.org/hco/10/GRCh38#117070131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59107824-A-C

117070300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59107987-T-C

117071251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59108664-T-G

http://identifiers.org/hco/10/GRCh38#117071288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59108701-C-A

117074493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59112576-A-G

http://identifiers.org/hco/10/GRCh38#117074539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59112624-A-C

117088978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59114715-G-A

117090637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59116498-A-T

117090684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59116545-A-G

117090809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59116664-G-A

117090811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59116666-A-G

117090822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59116677-G-T

117092468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59118144-C-T

117092530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59118204-A-G

117092783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59118443-G-A

http://identifiers.org/hco/10/GRCh38#117092857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59118512-A-C

117093614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59120347-C-T

117093724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59120409-T-C

117094296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59121089-T-G

117094370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59121176-G-A

117094925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59121706-C-T

117095223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59122004-C-T

117096270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59123053-C-G

117096324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59123107-T-C

117096470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59123269-G-A

117096594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59123388-T-C

117097034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59123804-C-T

117097040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59123810-C-G

117097147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59123908-G-A

117097172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59123947-C-T

117097301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59124066-G-C

117100389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59127027-C-T

117100668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59127312-C-G

117100997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59127767-G-C

117100997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59127767-G-T

117101205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59127974-C-T

117101478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128300-C-T

117101496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128318-G-A

117101538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128374-G-A

http://identifiers.org/hco/10/GRCh38#117101574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59128406-C-A

117101623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128448-A-G

117101623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128448-A-T

117101632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128456-G-A

117101676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128494-A-G

117101677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128495-T-G

117101742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128543-C-T

117101778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128578-A-G

117101808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128613-T-C

117101948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128748-T-A

117101964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59128768-G-A

117102359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59129160-A-G

117102359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59129160-A-T

117102483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59129284-G-A

117102545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59129348-C-T

117103036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59129878-C-T

117105033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59131012-C-G

117105033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59131012-C-T

http://identifiers.org/hco/10/GRCh38#117105074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59131052-C-A

117107145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59133406-G-T

117107606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59133673-T-G

117107728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59133792-C-G

117107728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59133792-C-T

117108012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59134203-A-G

117108013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59134204-T-C

117112412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59138672-A-G

117112476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59138730-A-G

117112808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59139048-G-A

117113282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59139496-G-A

117113366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59139542-G-A

117113584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59139758-C-T

117114479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59140657-T-G

117114536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59140716-C-T

117114588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59140768-C-T

117114823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59140946-G-T

117114916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141038-G-C

117115065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141179-T-G

117115072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141186-C-T

117115099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141212-A-G

117115154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141268-C-T

117115213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141319-C-T

117115588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141783-T-C

117115641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141835-C-T

117115682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141876-T-C

117115684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59141878-T-C

117124410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59143944-A-G

117124429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29319
most severe consequence: intron variant
orthologous variants: 59143962-C-G