130143975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26148405-G-C

130144337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26148046-A-G

130144431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26147954-T-C

130144435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 26147950-T-C

http://identifiers.org/hco/6/GRCh38#130144445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26147934-C-A

130144500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26147881-G-C

130144515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26147874-T-C

130144629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26147766-G-A

130144647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26147748-T-C

130144647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26147748-T-G

130144660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26147735-C-T

130144757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26147638-C-T

130144797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26147598-A-G

http://identifiers.org/hco/6/GRCh38#130144837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26147556-C-A

130144837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147556-C-G

130144837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147556-C-T

130144854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147539-A-G

http://identifiers.org/hco/6/GRCh38#130145279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26147438-A-C

130145279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147438-A-G

130145280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147437-T-A

130145280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147437-T-C

130145280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147437-T-G

130145282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147435-T-A

130145282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147435-T-C

130145282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147435-T-G

130145283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147434-A-G

http://identifiers.org/hco/6/GRCh38#130145287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26147430-A-C

130145287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147430-A-G

130145323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147401-A-G

http://identifiers.org/hco/6/GRCh38#130145516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26147190-C-A

130145516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147190-C-T

http://identifiers.org/hco/6/GRCh38#130145522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26147184-C-A

130145522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147184-C-G

130145522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147184-C-T

130146105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26146062-T-C

130146241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145917-G-A

130146241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145917-G-T

130146251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145907-A-G

http://identifiers.org/hco/6/GRCh38#130146287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26145865-A-C

130146287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145865-A-T

http://identifiers.org/hco/6/GRCh38#130146288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26145864-C-A

130146288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145864-C-G

130146288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145864-C-T

130146300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145852-T-C

130146319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145839-G-T

130146368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26145803-A-G

http://identifiers.org/hco/6/GRCh38#130147169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26144367-C-A

130147251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26144290-T-C

130147251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26144290-T-G

http://identifiers.org/hco/6/GRCh38#130147292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26144254-A-C

130147369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26144172-C-T

130147375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26144166-A-T

130147410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26144130-G-A

130147800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26143796-C-G

130147961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26143672-G-A

130151916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26141327-T-C

130151935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26141308-C-T

130154340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26140053-T-C

130155078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26139608-A-G

130155078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26139608-A-T

130155121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26139562-G-A

130155121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26139562-G-T

130155177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26139502-C-T

http://identifiers.org/hco/6/GRCh38#130155670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26138580-C-A

130155802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26138453-G-A

130155989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26138290-A-G

130156012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26138267-A-G

130156616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26137947-G-A

130157133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26137892-T-C

130157150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26137876-G-T

http://identifiers.org/hco/6/GRCh38#130157216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26137815-A-C

http://identifiers.org/hco/6/GRCh38#130157975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26137170-C-A

130157985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26137160-T-A

130158485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26136738-A-G

130161659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135532-T-C

http://identifiers.org/hco/6/GRCh38#130161766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26135451-C-A

130161766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135451-C-T

http://identifiers.org/hco/6/GRCh38#130161774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26135440-C-A

130161841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135371-T-C

130161841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135371-T-G

130161907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135313-G-A

130161907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135313-G-T

130161908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135312-T-G

http://identifiers.org/hco/6/GRCh38#130161932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26135283-C-A

130161932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135283-C-T

130161938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135277-A-G

http://identifiers.org/hco/6/GRCh38#130161970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26135263-C-A

130161970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135263-C-T

130161980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135253-A-G

130162009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135225-G-A

130162020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135215-A-G

130162034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135201-T-C

130162037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135198-A-G

130162114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135135-A-G

130162211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135084-G-C

130162258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135037-T-C

130162258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26135037-T-G

130162397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26134895-A-T

130163287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26133216-G-C

130163333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26133170-C-G

130163381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26133121-T-A

130163426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26133077-A-G

130163734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26132772-G-T

130163838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26132683-T-C

130164582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26132043-C-T

130168028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26131308-G-A

130168028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26131308-G-C

130168028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26131308-G-T

130168700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130983-A-G

130169278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130743-C-G

130169295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130735-A-G

130169322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130718-T-C

130169324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130716-C-G

130169386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130666-C-T

130169470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130581-T-C

130169636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130423-G-A

130169636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130423-G-T

http://identifiers.org/hco/6/GRCh38#130169769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26130305-C-A

130169814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130262-C-T

130169824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130261-G-A

130169825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26130260-C-T

130174713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26129150-A-G

130174883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26128976-G-A

130175152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26128718-G-T

130175154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26128716-T-A

130175201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26128655-A-T

130175445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26128444-G-A

130175536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26128091-T-C

130175604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26128022-A-G

http://identifiers.org/hco/6/GRCh38#130175785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26127860-C-A

130175785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26127860-C-T

130176157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26127507-T-A

130176157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26127507-T-C

130176168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26127496-T-C

130176175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26127489-A-T

130176226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26127447-G-A

130178839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26125878-G-A

130179052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26125686-T-C

130179101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26125650-T-C

http://identifiers.org/hco/6/GRCh38#130179446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26125401-A-C

http://identifiers.org/hco/6/GRCh38#130179522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26125292-C-A

130179522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26125292-C-T

http://identifiers.org/hco/6/GRCh38#130179613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26125179-A-C

130179627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26125165-G-A

130179627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26125165-G-T

130179694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26125106-C-T

130181478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26123930-G-C

130181511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26123901-C-T

130182214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26123206-G-A

130182318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 26123121-G-T

130182366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26123068-T-C

130182375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26123059-C-T

130182419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26123022-C-T

130182570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122915-G-C

130182573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122912-A-T

130182641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122857-A-G

130182641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122857-A-T

130182883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122772-G-A

130182883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122772-G-T

130182899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122753-G-A

130182903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122749-C-T

130182959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122704-G-A

130182959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122704-G-T

130182978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26122685-T-C

130183205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26122472-G-A

http://identifiers.org/hco/6/GRCh38#130183321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26122353-A-C

130183321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26122353-A-T

130183457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26122263-C-T

130183463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26122257-G-T

130183489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26122216-A-G

130183517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26122186-C-G

130183517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26122186-C-T

http://identifiers.org/hco/6/GRCh38#130183558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26122141-C-A

130183980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26121680-G-A

130183980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26121680-G-C

130183980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26121680-G-T

130184086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26121542-G-A

130184086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26121542-G-T

130184389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26120609-T-C

130184494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26120506-C-G

130184507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26120493-T-A

130184614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26120386-C-T

http://identifiers.org/hco/6/GRCh38#130184635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26120365-A-C

130184635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26120365-A-G

http://identifiers.org/hco/6/GRCh38#130184704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26120296-A-C

130185003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26120075-C-T

130185182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26119904-A-G

130185187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26119899-G-A

130186267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26119478-A-T

130186411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26119355-T-C

130186685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26119112-A-T

130186740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26119057-G-A

130186740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26119057-G-T

130186743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26119054-G-T

130187903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26118015-T-C

130188182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26117577-C-G

130188250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26117507-G-A

130188258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26117499-T-G

130188259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26117498-C-G

130188259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26117498-C-T

130189395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26116169-C-T

130189409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26116156-C-T

130189465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26116102-T-C

130189667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26115923-A-G

130198516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26114925-G-A

130198516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26114925-G-T

130198603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26114838-T-C

130202640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113969-A-T

130202928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113795-G-A

130202976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26113749-A-G

130203325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113447-C-T

130203334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113441-G-T

http://identifiers.org/hco/6/GRCh38#130203349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26113430-C-A

130203414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113356-C-T

130203480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113292-A-T

130203496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113276-A-G

130203504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113268-T-C

130203629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113104-C-G

130203750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26113000-T-C

http://identifiers.org/hco/6/GRCh38#130204138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26112552-A-C

130204140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112550-C-T

130204150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112542-C-T

130204205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112491-C-T

130204214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112482-C-G

130204286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112422-A-G

130204768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112178-T-C

http://identifiers.org/hco/6/GRCh38#130204790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26112156-C-A

http://identifiers.org/hco/6/GRCh38#130204792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26112154-C-A

130204797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112149-G-A

130204797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112149-G-T

130204888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112072-G-T

130204924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26112034-A-T

130205025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26111951-T-G

130205029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26111947-A-G

130205039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26111936-C-G

130205039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26111936-C-T

http://identifiers.org/hco/6/GRCh38#130205101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26111873-A-C

130205101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26111873-A-G

130205981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26111089-G-T

130205988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26111082-C-T

130205998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26111071-C-T

130206211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26110910-C-T

http://identifiers.org/hco/6/GRCh38#130206334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26110806-C-A

130206343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26110797-G-C

130206399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26110747-G-C

130206543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26110645-C-G

130206543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26110645-C-T

130206585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26110603-A-G

130209362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109648-T-C

130209362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109648-T-G

130209402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109609-T-C

130209459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109558-T-C

130209465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109552-T-A

http://identifiers.org/hco/6/GRCh38#130209480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26109537-A-C

130209513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26109505-T-C

130209527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26109491-A-T

130209549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26109472-T-A

130209573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26109451-T-A

130209573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26109451-T-C

130209591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26109433-G-A

130209591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26109433-G-T

130209623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109401-G-A

130209623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109401-G-T

130209646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109379-G-A

130209646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109379-G-T

130209653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109372-G-A

130209653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109372-G-T

http://identifiers.org/hco/6/GRCh38#130209656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26109369-C-A

http://identifiers.org/hco/6/GRCh38#130209666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26109359-A-C

130209666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109359-A-G

130209829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26109234-A-G

http://identifiers.org/hco/6/GRCh38#130212314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26108717-C-A

130212316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26108715-G-A

130212544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26108489-C-T

130212589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26108447-C-T

http://identifiers.org/hco/6/GRCh38#130212691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26108344-C-A

130212691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26108344-C-T

http://identifiers.org/hco/6/GRCh38#130212715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26108321-A-C

130212716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26108320-C-G

130212905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26108114-T-C

http://identifiers.org/hco/6/GRCh38#130213290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26107887-C-A

130213290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107887-C-T

130213473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107779-A-G

130213630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107592-C-T

http://identifiers.org/hco/6/GRCh38#130213927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26107300-C-A

130213981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107250-A-T

130214127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107118-G-A

http://identifiers.org/hco/6/GRCh38#130214198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26107047-A-C

130214207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107038-A-G

130214207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107038-A-T

130214237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107008-G-A

130214237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26107008-G-T

130214277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106968-T-C

130214292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106958-G-A

130214292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106958-G-T

130214311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106939-A-T

http://identifiers.org/hco/6/GRCh38#130214317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26106933-C-A

130214317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106933-C-T

130214343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26106907-G-A

130214343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26106907-G-T

130214370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26106880-G-A

130214504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26106746-A-G

130214505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26106745-G-C

130214539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106714-A-G

http://identifiers.org/hco/6/GRCh38#130214545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26106708-A-C

130214545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106708-A-G

130214545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106708-A-T

130214591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106662-G-A

130214591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106662-G-T

130214933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106340-A-G

http://identifiers.org/hco/6/GRCh38#130215080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26106210-C-A

130215080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106210-C-T

130215137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106160-G-A

130215137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106160-G-T

130215173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106124-T-C

130215174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26106123-T-C

130215325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26105900-G-C

130215325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26105900-G-T

130215440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26105786-C-G

130215440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26105786-C-T

130215506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26105727-T-C

http://identifiers.org/hco/6/GRCh38#130215584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26105660-C-A

130215584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26105660-C-G

130215584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26105660-C-T

130215855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26105426-C-T

http://identifiers.org/hco/6/GRCh38#130215917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26105370-C-A

130215917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26105370-C-G

130216040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26105036-A-G

http://identifiers.org/hco/6/GRCh38#130216104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26104971-C-A

130216138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26104938-G-C

130216202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26104875-T-A

130216292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26104798-C-T

130216343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26104747-T-A

130216408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26104687-G-T

130216908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26104204-A-G

130217139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26103950-G-A

130217144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26103945-T-C

130217204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26103886-G-A

130217711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26103497-G-A

130220421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26101742-T-G

130220460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26101705-T-G

130220468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26101697-C-T

130220516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26101639-T-C

130220688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26101528-T-G

130228440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26093906-A-G

130228442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26093904-G-A

130228484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26093870-A-G

130228484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26093870-A-T

130228826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26093619-C-T

130229090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26093398-A-G

130229511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26092214-G-A

130229656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26092073-A-G

130229888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26091868-A-G

130229896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26091861-T-C

130233532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26087815-G-A

130234051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26082404-A-T

130234338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26082183-A-G

130234423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26082097-C-G

130234590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26081979-G-A

130234590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26081979-G-C

130234668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26081901-G-C

130234782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26081782-T-G

130235225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26081516-G-T

130235386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26081393-A-G

http://identifiers.org/hco/6/GRCh38#130235655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26081019-C-A

130235756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26080934-A-T

130235912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26080780-A-G

130235930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26080762-A-G

130236957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26079346-T-C

130240224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26078105-T-A

130240433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26077902-G-T

130240569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26077741-T-A

130240882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26077462-C-T

http://identifiers.org/hco/6/GRCh38#130242767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26075382-A-C

130242768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26075381-C-T

130243315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26074923-A-G

130243454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26074597-T-G

130243605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26074312-T-C

130243864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26074056-T-C

130243867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26074053-A-G

130244028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073898-A-G

130244052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073874-T-C

130244119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073807-A-G

130244155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073771-T-C

130244183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073743-T-A

130244200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073726-A-G

130244292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073628-C-T

http://identifiers.org/hco/6/GRCh38#130244315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26073601-C-A

130244315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073601-C-T

130244408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26073510-C-T

130244970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26072774-A-T

130245261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26072496-A-G

130247965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26068145-T-C

130248616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26067191-C-G

130248747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26067052-G-A

130249452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26066401-A-G

130249453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26066400-A-G

130256361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26061641-A-G

http://identifiers.org/hco/6/GRCh38#130256362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26061640-C-A

130256362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26061640-C-T

130256542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26061500-G-T

130256550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26061492-G-T

130257050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26061049-C-G

130286576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26041492-C-T

130286583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26041485-T-C

130286615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26041453-C-G

130286679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26041386-C-T

130287155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26041224-T-C

http://identifiers.org/hco/6/GRCh38#130287157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26041222-C-A

130287358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26040937-T-A

130287367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26040928-T-A

http://identifiers.org/hco/6/GRCh38#130288240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26040057-C-A

130288305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26039994-T-G

130288409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26039885-A-T

130288687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26039668-T-C

130288981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26039025-C-G

130289421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26038608-T-A

130289452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26038583-A-G

http://identifiers.org/hco/6/GRCh38#130292073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26034175-A-C

130292152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26034101-G-A

130292153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26034100-G-T

http://identifiers.org/hco/6/GRCh38#130292159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26034094-C-A

130292286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26034022-T-G

130294255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26033635-T-C

130294380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26033528-T-C

130294459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26033450-T-C

130294502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26033406-G-A

130294502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26033406-G-C

130294846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26033081-G-A

130294846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26033081-G-T

130309259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26029286-G-T

http://identifiers.org/hco/6/GRCh38#130309397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26029221-C-A

130309673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26028692-T-C

130309708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26028662-G-C

130309738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26028657-G-A

130309839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26028571-C-G

130309887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26028525-C-G

130309935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26028494-G-A

130310218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26028247-A-G

130310218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26028247-A-T

130310226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26028239-C-T

130310416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26028056-A-G

130310655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26027817-C-T

http://identifiers.org/hco/6/GRCh38#130310777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26027696-C-A

130310812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26027661-A-G

130310965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26027520-G-A

130310985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26027505-C-T

http://identifiers.org/hco/6/GRCh38#130311207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26027347-A-C

130311451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26027132-C-G

130311501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26027082-T-C

130311518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26027056-G-T

130312421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26024316-A-G

130312443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26024298-T-G

130312503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26024245-G-A

130312978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26023606-C-T

130312999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26023586-G-A

130313158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26023422-T-A

130313158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26023422-T-C

130313202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26023366-T-C

130313312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26023133-A-G

130313337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26023121-T-A

130313344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26023114-A-G

130313400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26023075-T-C

http://identifiers.org/hco/6/GRCh38#130313535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26022997-A-C

130313548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26022984-G-C

130313747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26022821-C-T

http://identifiers.org/hco/6/GRCh38#130313997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26022597-C-A

130313997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26022597-C-T

130314104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26022490-A-G

130314149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26022445-G-A

130314359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26022239-A-G

130314880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26021579-G-C

130314888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26021573-G-A

http://identifiers.org/hco/6/GRCh38#130315358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26021065-A-C

http://identifiers.org/hco/6/GRCh38#130315426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26020999-A-C

130315560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26020868-C-T

130316358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26019600-T-A

130316358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26019600-T-G

130316785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26019196-G-A

130316800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26019181-A-G

130316925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26019061-C-T

130316979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26019009-T-A

130316979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26019009-T-C

130317158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26018834-C-T

130317297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26018712-G-A

130318109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26018074-G-A

130322843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26015546-T-A

130322927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26015465-G-A

130323352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26015017-C-T

130323875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26014689-T-C

130324178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 26014378-G-A

130324703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron_variant, undefined
orthologous variants: 25999223-T-A

130325462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998796-G-A

130325462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998796-G-T

130325699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998647-C-T

130325705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998641-A-G

130326021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998278-G-A

130326072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998232-T-C

130326159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998151-G-A

130326160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998150-A-G

130326195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998114-T-G

130326224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998086-T-C

130326234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998076-A-G

130326271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25998046-T-C

130326361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25997839-C-T

http://identifiers.org/hco/6/GRCh38#130326389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25997728-C-A

130326389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25997728-C-T

130326390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25997727-T-A

130326427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25997690-T-A

130326472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25997646-C-T

130326875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25997293-G-A

130326938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25997229-T-A

http://identifiers.org/hco/6/GRCh38#130327123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25996910-C-A

130327189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25996847-A-G

130327652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25996427-C-T

130327790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25996314-C-T

130328005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25996119-C-G

http://identifiers.org/hco/6/GRCh38#130328040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25996086-C-A

130328040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25996086-C-T

130328208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25995929-G-A

130328566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25995606-C-G

http://identifiers.org/hco/6/GRCh38#130328915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25995248-A-C

130329048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994972-C-T

http://identifiers.org/hco/6/GRCh38#130329075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25994945-C-A

130329110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994752-G-A

http://identifiers.org/hco/6/GRCh38#130329134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25994707-C-A

130329169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994672-A-T

130329193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994647-G-C

130329207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994633-T-C

130329250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994591-T-A

130329250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994591-T-C

130330192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994345-C-T

130330209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25994328-G-A

130331029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25993587-G-A

130331029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25993587-G-T

130331110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25993472-G-A

http://identifiers.org/hco/6/GRCh38#130332013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25992455-A-C

http://identifiers.org/hco/6/GRCh38#130332254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25992248-C-A

130332278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25992224-G-C

130332375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25992124-A-G

130332497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25992017-T-C

130332677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25991856-C-T

130332694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25991847-A-G

130332729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25991812-T-A

130332735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25991806-A-G

130332996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25991263-G-C

http://identifiers.org/hco/6/GRCh38#130333041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25991174-A-C

130333041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25991174-A-G

130333259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25990986-G-A

130333592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25990692-T-C

130333733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25990418-A-G

130333835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25980587-G-T

130334002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25980424-T-C

130334113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25980315-A-G

130334815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25979714-T-A

130334815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25979714-T-C

130334836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25979694-G-A

130334955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25979575-T-G

130335113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25979434-C-T

130335206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25979340-T-C

http://identifiers.org/hco/6/GRCh38#130335436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25979124-C-A

130335584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25978979-G-C

130340026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25977404-C-T

130340301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25977245-G-C

130340397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25977105-C-G

130340729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25976778-C-T

http://identifiers.org/hco/6/GRCh38#130341047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25976456-C-A

130341047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25976456-C-T

130341074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25976430-G-A

130341080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25976427-C-T

130341126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25976385-T-G

130341151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25976366-G-A

130341488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25976066-C-T

130341556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25976014-A-G

130341850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25975777-G-A

130341989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25975640-T-G

130342003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25975626-C-T

130342302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25975346-T-C

130342335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25975312-G-T

130342537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25975146-G-A

http://identifiers.org/hco/6/GRCh38#130342585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25975103-C-A

130342796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25974951-C-T

130345653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25972469-A-T

130345655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25972467-G-A

130346034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25972094-C-T

http://identifiers.org/hco/6/GRCh38#130352234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25972053-A-C

130352434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25971452-A-G

130353071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25970786-A-G

130353209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25970667-T-C

130353419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25970516-T-C

130353464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25970470-T-C

130353697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25970109-G-A

130353744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25970062-A-G

130353745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25970061-A-G

http://identifiers.org/hco/6/GRCh38#130353772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25970034-A-C

130355001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25969909-T-C

130355453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25969787-A-T

130355665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25969580-A-G

130355860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25969395-G-A

130356296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25968836-T-G

130356305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25968816-G-A

130356579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25968558-T-G

130358379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25963260-C-G

130358379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25963260-C-T

130358468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25963165-G-A

130358814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25961895-C-T

130359246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25961803-T-C

130359270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25961778-T-C

130359289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25961760-T-C

130359333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25961721-G-A

130361851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25958639-T-C

http://identifiers.org/hco/6/GRCh38#130362146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25958364-C-A

130362146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25958364-C-T

130362391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25958157-G-A

130362643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957887-G-T

130362838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957706-T-C

130362838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957706-T-G

130362921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957634-C-T

130362936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957613-G-A

130362936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957613-G-T

130363079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957471-T-C

130363097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957454-C-T

130363244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957313-G-T

130363336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25957013-C-T

130363478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25956875-T-G

130363511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25956841-T-C

130364040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25956331-C-T

130364536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25955867-C-T

130364537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25955866-T-G

130364651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25955748-T-C

130364857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: intron variant
orthologous variants: 25955542-T-C

130365118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: splice donor variant
orthologous variants: 25955325-A-G

http://identifiers.org/hco/6/GRCh38#130365384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#25955058-C-A

130365384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25955058-C-G

130365384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25955058-C-T

130365490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25954953-G-A

130365490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25954953-G-C

130365490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25954953-G-T

130365570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25954872-G-A

130365592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25954850-G-A

130365609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25954834-G-T

130365683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21574
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25954769-C-G