5545187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370209-A-G

5545360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370270-A-G

http://identifiers.org/hco/20/GRCh38#5545374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132370284-C-A

5545374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370284-C-T

5545468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370353-G-A

5545468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370353-G-C

5545468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370353-G-T

5545530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370399-G-T

http://identifiers.org/hco/20/GRCh38#5545544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132370413-C-A

5545544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370413-C-T

5545637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370497-G-T

5545734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370543-T-C

http://identifiers.org/hco/20/GRCh38#5545776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132370573-C-A

5545776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370573-C-T

http://identifiers.org/hco/20/GRCh38#5545855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132370639-C-A

5545855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370639-C-G

5545855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370639-C-T

5545914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370682-G-T

5545974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370729-G-A

5545974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370729-G-T

5546038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370773-C-T

5546062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132370788-A-T

5546288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132371166-G-A

5547140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132371982-G-A

5547140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132371982-G-T

5547608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132372424-G-A

5547608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132372424-G-T

5547624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132372439-G-A

5547624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132372439-G-C

5547624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132372439-G-T

http://identifiers.org/hco/20/GRCh38#5547633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132372445-C-A

5547633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132372445-C-T

http://identifiers.org/hco/20/GRCh38#5547673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132372485-C-A

5547802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132372614-T-C

5548080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132372864-C-T

5552320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132374050-A-T

5552332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132374062-T-C

5552431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132374158-T-C

5552502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132374232-T-G

5552598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132374321-T-C

5552747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132374518-G-C

5552870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132374709-C-T

5556926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375067-T-C

5556955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375095-T-C

5556974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375114-G-A

5557027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375158-T-G

5557656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375775-A-G

5557837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375890-G-T

http://identifiers.org/hco/20/GRCh38#5557922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132375971-A-C

5557922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375971-A-G

5558112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132376161-G-A

5558112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132376161-G-T

5558195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132376231-C-G

5558195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132376231-C-T

5558207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132376244-A-G

5558681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132376615-T-C

5559917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132377260-A-G

5559917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132377260-A-T

5561429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132378581-G-A

5561429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132378581-G-T

5561638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132378778-T-A

5561638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132378778-T-C

5561912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132379051-A-T

http://identifiers.org/hco/20/GRCh38#5564926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132379911-C-A

5564997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132379981-G-A

5564997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132379981-G-T

http://identifiers.org/hco/20/GRCh38#5565093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132380078-C-A

5565093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132380078-C-T

5565101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132380086-C-T

5565824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132380829-T-C

5566168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132381092-T-C

5566169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132381093-A-G

5566299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132381205-T-C

5566410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132381347-C-T

5566628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132381739-T-C

5566726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132381812-T-C

5567335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382091-T-C

http://identifiers.org/hco/20/GRCh38#5567371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132382098-C-A

http://identifiers.org/hco/20/GRCh38#5567426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132382151-C-A

5567426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382151-C-T

5567658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382342-G-T

http://identifiers.org/hco/20/GRCh38#5567677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132382361-C-A

5567677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382361-C-T

5567727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382410-G-A

5567727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382410-G-T

5567835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 132382626-G-T

5567871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382659-T-A

5567871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382659-T-C

5567897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382697-T-A

5567897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132382697-T-C

5568298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132383053-A-T

5568445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132383200-G-A

5568445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132383200-G-T

5568606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132383363-G-C

5569787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132383853-T-C

5569868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132383923-G-T

5569960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132384015-G-A

http://identifiers.org/hco/20/GRCh38#5570066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132384102-A-C

5570066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132384102-A-G

5570237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 132384253-A-G

http://identifiers.org/hco/20/GRCh38#5570248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132384269-A-C

5570248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132384269-A-G

5570288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132384314-C-T

5570307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132384331-G-A

5570307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132384331-G-T

http://identifiers.org/hco/20/GRCh38#5570440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132384479-A-C

5570654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132384646-T-G

5574091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132386463-T-A

5574144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132386523-T-A

5574249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132386616-T-A

5575228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132388549-T-C

5575554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132388902-G-A

5575554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132388902-G-T

5575710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132389060-T-G

http://identifiers.org/hco/20/GRCh38#5575754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132389107-A-C

http://identifiers.org/hco/20/GRCh38#5575778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132389411-C-A

5575778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132389411-C-G

5575778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132389411-C-T

5575880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132389541-A-G

5577896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132391058-T-C

5577897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132391059-T-G

5578348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132392202-T-C

5578401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132392255-T-C

5578524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132392378-C-T

5578575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132392438-G-A

5578596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132392459-T-C

http://identifiers.org/hco/20/GRCh38#5578621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132392484-A-C

5578621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132392484-A-G

5578633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132392495-G-C

5579783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395689-T-C

5579850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395755-G-A

5579850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395755-G-C

5579867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395772-T-A

5579867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395772-T-C

5579942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395811-T-A

5579942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395811-T-C

5579942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395811-T-G

5579947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395816-T-A

5579966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395835-G-A

5579966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132395835-G-T

5580046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132395915-C-T

5580166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132396034-T-A

5580166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132396034-T-C

http://identifiers.org/hco/20/GRCh38#5580195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132396059-A-C

5580195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132396059-A-T

5582042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132397788-C-T

5582047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132397793-G-A

5582047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132397793-G-C

5582054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132397800-C-T

5582093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132397820-G-T

5582103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132397830-G-A

5582103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132397830-G-T

http://identifiers.org/hco/20/GRCh38#5582140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132397868-C-A

5582140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132397868-C-T

http://identifiers.org/hco/20/GRCh38#5582201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132397906-A-C

http://identifiers.org/hco/20/GRCh38#5582205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132397910-A-C

5582458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132398129-C-T

5583492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132398217-G-A

5583504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132398229-C-T

http://identifiers.org/hco/20/GRCh38#5583565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132398289-A-C

http://identifiers.org/hco/20/GRCh38#5584724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132399262-C-A

http://identifiers.org/hco/20/GRCh38#5584753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132399291-A-C

5584950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132399442-T-C

http://identifiers.org/hco/20/GRCh38#5585031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132399519-A-C

5585061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132399547-A-G

5585313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132399790-C-T

5585438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132399905-C-T

5585880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132400263-G-A

5585880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132400263-G-T

http://identifiers.org/hco/20/GRCh38#5586122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132400455-C-A

5586122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132400455-C-T

5586143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132400476-T-C

5587070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132401359-C-T

5587207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132401458-A-G

5587239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132401466-C-T

5588868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132402178-G-A

http://identifiers.org/hco/20/GRCh38#5589117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132402402-A-C

5589968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132403049-A-G

5590873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132403757-G-C

http://identifiers.org/hco/20/GRCh38#5592108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132405437-C-A

5592396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132405694-G-A

5592513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132405786-A-T

5593020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132406242-G-A

5593219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132406442-C-T

http://identifiers.org/hco/20/GRCh38#5593260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132406483-C-A

5593260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132406483-C-T

5593556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132406769-T-C

5593558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132406771-G-A

5593558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132406771-G-T

5597845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132407573-C-T

5597856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132407587-A-G

5597857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132407588-A-G

5597996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132407760-T-C

5598634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132410446-T-A

5598691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132410506-C-T

http://identifiers.org/hco/20/GRCh38#5598863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132410682-C-A

5598863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132410682-C-T

http://identifiers.org/hco/20/GRCh38#5598908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132410740-A-C

5598925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132410757-G-T

5598936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132410783-A-G

5602362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132412251-G-C

5602448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132412335-G-A

http://identifiers.org/hco/20/GRCh38#5603677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132413097-C-A

5603677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132413097-C-G

5603746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132413186-C-T

5603767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132413240-G-A

5603767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132413240-G-T

5603770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132413243-G-A

5603770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132413243-G-T

5603908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132413360-G-A

5604461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132414201-A-G

5605347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132415455-G-A

5605413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132415521-C-T

http://identifiers.org/hco/20/GRCh38#5606289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#132416092-A-C

5606306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132416104-C-T

5606335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132416141-C-T

5607270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132416845-C-G

5607985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132417491-A-G

5608000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132417506-T-C

5608235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132417722-T-C

5608287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132417773-T-A

5608287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132417773-T-C

5608291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132417777-C-T

5608986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132418519-T-C

5609065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132418607-G-A

5609309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132418835-G-C

5609823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 132419261-T-G

5609864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 132419299-G-A

5609864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 132419299-G-T

5610856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 132419986-G-T

5610961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 5 prime UTR variant
orthologous variants: 132420073-T-C

5610961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 5 prime UTR variant
orthologous variants: 132420073-T-G

http://identifiers.org/hco/20/GRCh38#5610964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#132420076-C-A

5610964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26957
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 132420076-C-T