11823428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6134891-G-A

11823428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6134891-G-T

http://identifiers.org/hco/10/GRCh38#11823447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6134872-C-A

11823447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6134872-C-T

11823502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6134824-T-C

11823502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6134824-T-G

11823558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134769-G-A

11823558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134769-G-T

11823574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6134751-G-T

11823636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134710-G-C

11823895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134492-G-C

11823902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134485-C-T

11823925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134449-C-G

11823925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134449-C-T

http://identifiers.org/hco/10/GRCh38#11824018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6134354-C-A

11824478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133968-G-A

11824628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133807-T-C

11824928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133503-C-G

11824928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133503-C-T

11824958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133471-C-G

11824970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133459-A-G

11825302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133122-G-A

11825418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133007-T-C

11825605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6132886-G-A

11827646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6130450-G-T

11828062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6130195-C-G

11828397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6129850-T-A

11831109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6129240-C-T

11831188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6129192-C-T

11831488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6128922-A-G

11831717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6128686-G-A

11831764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6128637-G-A

11831764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6128637-G-T

11831963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6128458-C-T

11835349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6126383-A-G

11835398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6126332-A-G

11835477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6126264-G-A

11835477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6126264-G-T

11835624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6125956-T-G

http://identifiers.org/hco/10/GRCh38#11850667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6122044-C-A

11850754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121980-A-G

11850832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121905-G-T

11850901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121838-G-A

11850901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121838-G-C

11850928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121810-G-A

11850928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121810-G-T

11851413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121106-T-C

http://identifiers.org/hco/10/GRCh38#11851436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6121088-A-C

11851436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121088-A-G

http://identifiers.org/hco/10/GRCh38#11851457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6121074-C-A

11851457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121074-C-T

11851488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121051-A-T

11851568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120954-A-G

11851594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120928-A-G

11851647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120872-G-T

11851648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120871-G-A

11851697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120823-G-A

11851697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120823-G-C

11851697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120823-G-T

11851733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120767-G-A

11851733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120767-G-C

11851733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120767-G-T

11851767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6120730-A-G

11852031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6118885-C-T

11852113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6118804-C-T

11852193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6118724-C-T

11852220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118697-G-A

http://identifiers.org/hco/10/GRCh38#11852344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6118616-C-A

11852344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118616-C-G

11852355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118605-G-A

11852355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118605-G-T

11852509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118473-C-G

11852509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118473-C-T

11852552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118433-G-T

11856392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117994-G-A

11856392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117994-G-C

11856412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117974-G-A

11856527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117858-C-T

http://identifiers.org/hco/10/GRCh38#11856541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6117844-A-C

11856651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117735-C-G

http://identifiers.org/hco/10/GRCh38#11856724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6117673-C-A

11856724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117673-C-T

11856780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117659-A-G

11856996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117487-C-T

11857290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6117194-C-T

http://identifiers.org/hco/10/GRCh38#11866345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6108057-C-A

11866345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6108057-C-T

11866449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6107932-T-A

11866502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6107887-C-G

11866502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6107887-C-T

11866612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6107793-G-A

11866723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6107682-G-C

11866723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6107682-G-T

11866736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6107669-C-G

11868063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106915-A-G

11868091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106888-T-C

http://identifiers.org/hco/10/GRCh38#11868103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106879-A-C

11868103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106879-A-T

11868207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106776-C-T

11868221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106762-C-T

11868247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106737-A-G

11868332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106628-A-G

11868413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106561-C-T

11868431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106543-A-T

11869204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106450-G-A

11869219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106435-G-A

11869219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106435-G-T

http://identifiers.org/hco/10/GRCh38#11869264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106388-C-A

11869264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106388-C-T

11869271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106374-A-G

11869271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106374-A-T

11869297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106346-G-T

http://identifiers.org/hco/10/GRCh38#11869335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106311-C-A

11869335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106311-C-G

11869346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106300-G-T

11869392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6106261-G-A

11869392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6106261-G-T

http://identifiers.org/hco/10/GRCh38#11869413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106243-C-A

11869413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6106243-C-G

11869413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6106243-C-T

11869485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6106174-T-C

11869490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6106169-G-T

11869578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6106060-G-A

11869578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6106060-G-T

http://identifiers.org/hco/10/GRCh38#11869579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106059-C-A

11869579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6106059-C-T

http://identifiers.org/hco/10/GRCh38#11869597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106041-A-C

11869666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105969-T-C

http://identifiers.org/hco/10/GRCh38#11869737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105898-C-A

11869737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105898-C-T

http://identifiers.org/hco/10/GRCh38#11869744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105891-C-A

11869744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105891-C-G

11869744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105891-C-T

11869777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105858-A-G

11869793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105842-G-A

11869793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105842-G-C

11869793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105842-G-T

http://identifiers.org/hco/10/GRCh38#11869801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105834-A-C

11869801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105834-A-G

11869801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105834-A-T

11869814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105818-G-A

11869814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105818-G-T

11869870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105756-A-G

11869870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105756-A-T

11870011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105600-G-A

11870011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105600-G-T

11870067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105528-G-A

11870067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105528-G-C

11870067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105528-G-T

11870069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105526-G-A

11870069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105526-G-C

11870069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105526-G-T

http://identifiers.org/hco/10/GRCh38#11870070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105525-C-A

11870070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105525-C-G

11870070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105525-C-T

http://identifiers.org/hco/10/GRCh38#11870071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105524-C-A

11870071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105524-C-T

11870106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105477-G-A

11870106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105477-G-C

11870106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6105477-G-T

http://identifiers.org/hco/10/GRCh38#11870113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105465-C-A

11870113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105465-C-G

11870113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105465-C-T

http://identifiers.org/hco/10/GRCh38#11870114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105464-C-A

11870114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105464-C-G

11870114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105464-C-T

11870201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105377-T-C

11870227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105351-A-G

http://identifiers.org/hco/10/GRCh38#11870236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105342-C-A

11870236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105342-C-T

http://identifiers.org/hco/10/GRCh38#11870266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105303-A-C

11870266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105303-A-G

11870296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6105270-T-C

11870414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6105137-G-A

11870414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6105137-G-C

11870414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6105137-G-T

http://identifiers.org/hco/10/GRCh38#11870431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105105-C-A

11870431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6105105-C-G

11870431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6105105-C-T

http://identifiers.org/hco/10/GRCh38#11870591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6104972-C-A

11870591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104972-C-T

11870597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104966-C-G

11870597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104966-C-T

11870829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104866-T-C

11870897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104773-G-A

11870897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104773-G-T

11870932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104741-T-C

11871053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104591-A-G

http://identifiers.org/hco/10/GRCh38#11871087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6104562-C-A

11871087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104562-C-T

11871088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104561-G-A

11871088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104561-G-T

11871098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104552-G-A

11871100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104550-T-C

11871100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104550-T-G

11871249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104395-G-T

11871299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104357-C-T

11871385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104303-C-T

http://identifiers.org/hco/10/GRCh38#11871557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6104139-C-A

11871665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6104037-C-T

11871850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6103848-G-C

http://identifiers.org/hco/10/GRCh38#11871862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6103836-C-A

11872029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6103680-T-C

11872208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6103531-G-A