16388036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140849177-C-T

16388039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140849174-G-A

16390551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 140848394-T-C

16390690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140848270-A-G

16390818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140848165-G-T

16390862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140848113-A-T

16390942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140848036-T-G

16390957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140848031-A-G

16390989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140848009-A-G

16391485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140847572-G-A

16391527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140847543-A-G

16392063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140847109-G-A

16392063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140847109-G-C

16392844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140846441-G-T

16393208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140846110-C-T

16393501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140845803-G-A

16393501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140845803-G-T

16393505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140845799-G-A

16393505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140845799-G-T

16394524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140843673-G-A

16395145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140843066-A-G

16395834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140842382-A-G

http://identifiers.org/hco/1/GRCh38#16395868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140842352-C-A

16395868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140842352-C-T

http://identifiers.org/hco/1/GRCh38#16396369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140841929-C-A

16396370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841928-A-G

16396738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140841605-G-A

http://identifiers.org/hco/1/GRCh38#16396763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140841583-C-A

16396763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841583-C-T

16396777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841577-C-T

http://identifiers.org/hco/1/GRCh38#16396798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140841556-C-A

16396798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140841556-C-G

16396859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841520-A-G

16396945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841445-G-T

16397078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841352-G-T

16397182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841306-G-A

16397182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841306-G-T

http://identifiers.org/hco/1/GRCh38#16397183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140841305-C-A

16397183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841305-C-T

16397202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841291-G-T

16397204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841289-A-G

16397319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841174-G-A

16397395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140841104-G-T

16397523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140840936-G-A

16397523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140840936-G-T

http://identifiers.org/hco/1/GRCh38#16397870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140840590-A-C

16397870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140840590-A-T

16398026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140840437-T-C

16398077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140840392-G-A

16398077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140840392-G-T

http://identifiers.org/hco/1/GRCh38#16398537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140840129-A-C

16398835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839892-G-A

http://identifiers.org/hco/1/GRCh38#16398888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140839833-A-C

16398888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839833-A-G

16398924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839804-G-A

16398924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839804-G-C

16398957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839775-G-A

16398957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839775-G-T

16399157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839620-A-G

16399244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839563-A-G

16399559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839260-G-A

16399559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839260-G-T

16399618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839220-G-T

http://identifiers.org/hco/1/GRCh38#16399653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140839187-C-A

16399653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140839187-C-G

16400502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140838908-G-A

16400502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140838908-G-C

16400502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140838908-G-T

16400669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140838792-A-G

http://identifiers.org/hco/1/GRCh38#16400701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140838772-C-A

16400701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140838772-C-T

16400836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140838633-G-A

16400852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 140838617-G-A

http://identifiers.org/hco/1/GRCh38#16400975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140838495-C-A

http://identifiers.org/hco/1/GRCh38#16403065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140835253-C-A

16403113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140835211-A-G

16403637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140834838-G-T

16403661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140834813-T-C

16403661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140834813-T-G

16403703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140834777-C-T

http://identifiers.org/hco/1/GRCh38#16403704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140834776-C-A

http://identifiers.org/hco/1/GRCh38#16403714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140834766-C-A

16403714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140834766-C-T

16403760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140834720-G-A

16403849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140834631-A-G

http://identifiers.org/hco/1/GRCh38#16404092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140834399-C-A

16404092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140834399-C-G

16404092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140834399-C-T

16405160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140832082-T-C

16405161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140832081-C-G

16405161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140832081-C-T

16408158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140831874-G-A

16408349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140831678-G-A

16408349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140831678-G-T

http://identifiers.org/hco/1/GRCh38#16408420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140831604-C-A

http://identifiers.org/hco/1/GRCh38#16408439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140831584-C-A

16409266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140831184-G-A

16409266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140831184-G-T

16409277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140831173-G-T

http://identifiers.org/hco/1/GRCh38#16409308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140831144-C-A

http://identifiers.org/hco/1/GRCh38#16409319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140831140-C-A

16409319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140831140-C-T

http://identifiers.org/hco/1/GRCh38#16409376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140831047-A-C

http://identifiers.org/hco/1/GRCh38#16409500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140830840-C-A

16409500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140830840-C-T

http://identifiers.org/hco/1/GRCh38#16409542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140830797-A-C

http://identifiers.org/hco/1/GRCh38#16409555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140830784-C-A

16409555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140830784-C-G

16409556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140830783-T-A

16409628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140830710-T-A

http://identifiers.org/hco/1/GRCh38#16409776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140830580-C-A

16409776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140830580-C-T

16410016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140830307-C-T

http://identifiers.org/hco/1/GRCh38#16410157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140830172-C-A

16410157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140830172-C-G

16410157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140830172-C-T

http://identifiers.org/hco/1/GRCh38#16410173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140830152-C-A

16410173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140830152-C-G

16410173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140830152-C-T

16410402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140829894-C-T

16410493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140829795-C-T

16419110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140829254-G-C

16419504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140828913-T-C

16419508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140828909-T-C

16419512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140828905-A-G

16421437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140825424-T-C

http://identifiers.org/hco/1/GRCh38#16421441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140825420-C-A

http://identifiers.org/hco/1/GRCh38#16421447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140825415-C-A

16421447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140825415-C-T

16421450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140825412-G-T

16421545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140825308-C-T

16421546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140825307-A-G

16421552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140825301-T-C

16421581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140825270-G-A

16421581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140825270-G-T

16421670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140825204-G-T

16421671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140825203-G-A

16421671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140825203-G-T

16421933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824406-C-T

16421989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824350-A-T

16422035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824304-T-C

16422035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824304-T-G

16422037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824302-G-A

16422037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824302-G-C

16422071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824268-G-A

16422071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824268-G-C

16422072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140824267-G-A

16422072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140824267-G-T

16422088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140824251-G-T

16422120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140824219-G-A

http://identifiers.org/hco/1/GRCh38#16425463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140822696-C-A

16425463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140822696-C-T

16425464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140822695-T-A

16425464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140822695-T-C

16425541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140822617-G-T

16425593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140822565-C-T

16425628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140822536-G-T

16425732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 140822459-C-T

16425735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140822456-G-T

16425742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140822449-T-C

16425798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140822393-G-A

16425798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140822393-G-C

16425798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140822393-G-T

16425812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140822379-A-G

16427709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140819800-T-G

16427740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140819753-A-G

16427904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140819529-C-G

http://identifiers.org/hco/1/GRCh38#16427912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140819521-C-A

16427934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140819499-G-T

16428056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140819377-T-C

16428097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140819350-G-A

16428097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140819350-G-T

16428182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140819287-G-C

16428368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140819126-C-T

16428546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140818829-T-C

16428596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140818772-G-A

16428596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140818772-G-T

16428833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140818555-T-C

16431325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140817818-G-A

16431352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140817791-T-C

16431444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817701-G-A

16431444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817701-G-T

16431475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817671-C-T

16431585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817585-G-A

16431654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817552-G-A

16431704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817519-A-G

16431754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817485-C-G

16431809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817437-G-A

16431816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140817431-T-C

16432653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816522-T-C

16432673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816503-T-C

16432678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816498-G-A

16432678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816498-G-C

16432678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816498-G-T

http://identifiers.org/hco/1/GRCh38#16432690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140816486-C-A

16432695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816481-T-C

16432711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816463-C-T

16432741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816433-G-C

http://identifiers.org/hco/1/GRCh38#16432760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140816418-C-A

16432761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816417-C-G

16432761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816417-C-T

16432871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 140816311-G-C

16432887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 140816297-G-A

16432925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 140816260-C-T

16432967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816208-G-T

http://identifiers.org/hco/1/GRCh38#16433063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140816107-C-A

16433063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816107-C-T

http://identifiers.org/hco/1/GRCh38#16433082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140816088-C-A

16433164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140816028-G-A

16433209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140815994-C-G

16433209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140815994-C-T

16433310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140815898-G-T

16433486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140815693-C-T

16433488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140815691-C-T