http://identifiers.org/hco/20/GRCh38#18587959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144441859-C-A

18587959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 144441859-C-G

18587959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 144441859-C-T

18587987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 144441886-T-C

18588043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144441940-G-A

18588043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144441940-G-T

18588046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144441943-G-A

18588046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144441943-G-C

18588046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144441943-G-T

http://identifiers.org/hco/20/GRCh38#18588057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144441953-C-A

18588057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144441953-C-T

18588133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442028-G-A

18588133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442028-G-C

18588133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442028-G-T

18588168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442059-G-A

18588168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442059-G-C

18588168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442059-G-T

18588171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442062-T-C

18588500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442357-C-T

18588626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144442488-T-G

http://identifiers.org/hco/20/GRCh38#18588646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144442508-C-A

18588646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144442508-C-G

18588705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442561-G-A

http://identifiers.org/hco/20/GRCh38#18588759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144442610-A-C

18588759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144442610-A-G

18588761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144442612-T-C

18588917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144442744-G-T

18589180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144443062-A-G

http://identifiers.org/hco/20/GRCh38#18589190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144443074-C-A

18589534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144443477-A-G

18589761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144443695-G-A

18593119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144445398-G-T

http://identifiers.org/hco/20/GRCh38#18593197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144445475-A-C

18594249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144446155-A-G

18594277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144446182-G-A

18594277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144446182-G-T

http://identifiers.org/hco/20/GRCh38#18594558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144446282-C-A

18594558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144446282-C-T

18595710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144458853-G-A

18595761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144458896-A-G

18595970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144459076-C-G

18595983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144459089-C-G

18595983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144459089-C-T

18596144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 144459250-T-C

18596189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 144459295-C-T

18610008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144461599-C-T

18610425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144461792-A-G

http://identifiers.org/hco/20/GRCh38#18610499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144461872-A-C

18611284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144462013-A-G

18611301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144462030-G-C

18612351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144462504-A-G

18613220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144463003-C-T

18613496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144463266-T-C

18615709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144464319-G-C

18615735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144464345-C-G

18615875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144464478-T-C

18617168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144466683-C-T

18617230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144466747-A-G

18617296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144466810-G-A

18623414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144469267-C-G

18623613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144469435-C-G

18623613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144469435-C-T

18623888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144469669-G-C

18623917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144469699-A-G

18623981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144469752-A-G

http://identifiers.org/hco/20/GRCh38#18624524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144474715-C-A

18624667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144474856-C-G

18624672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144474861-A-G

18624868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144475050-G-C

18624986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144475148-T-C

18625300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144475422-A-G

18625349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144475468-C-T

18625710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144475787-T-C

18625735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144475813-C-T

18625799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144475880-T-C

18626009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144476038-G-A

18626009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144476038-G-C

18626494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144476464-G-A

http://identifiers.org/hco/20/GRCh38#18626641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144476599-C-A

18626641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144476599-C-T

18626965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144476923-G-A

18626965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144476923-G-C

18626965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144476923-G-T

18627085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144477041-A-G

18627198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144477191-C-G

18627260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144477258-C-G

18627282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144477275-G-A

http://identifiers.org/hco/20/GRCh38#18627370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144477349-A-C

18627428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144477398-C-T

http://identifiers.org/hco/20/GRCh38#18628336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144477905-A-C

18628336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144477905-A-G

18628439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144477967-T-C

18630111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144478804-G-T

18630341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144479000-G-T

http://identifiers.org/hco/20/GRCh38#18630349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144479007-C-A

18630349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144479007-C-G

18630349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144479007-C-T

18630390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 144479013-C-T

18630391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 144479014-G-A

18630391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 144479014-G-C

18630399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 144479022-T-A

18630399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 144479022-T-C

18630399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 144479022-T-G

18630528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 144479105-T-C

18630528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 144479105-T-G

18630561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479134-A-G

18630615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479181-G-A

http://identifiers.org/hco/20/GRCh38#18630662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144479257-A-C

18630723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479332-G-A

18630723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479332-G-T

18630731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479341-G-T

http://identifiers.org/hco/20/GRCh38#18630741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144479351-C-A

18630831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479430-T-C

18630832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479431-T-C

18630900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479497-A-G

18630915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479511-A-G

18630915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479511-A-T

18630956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479554-G-A

18630956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479554-G-T

18631005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479602-G-T

18631045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479629-A-G

18631046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479630-A-T

18631065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479649-T-C

18631078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479668-T-G

18631093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479683-C-G

18631119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479707-C-T

18631130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479718-C-T

18631142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479730-T-C

http://identifiers.org/hco/20/GRCh38#18631161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144479749-C-A

18631161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144479749-C-T

18631360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480032-G-A

18631400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480077-T-C

18631400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480077-T-G

18631454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480152-T-C

18631510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480254-G-T

18631599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480330-G-T

http://identifiers.org/hco/20/GRCh38#18631625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144480360-C-A

18631625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480360-C-T

18631645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480377-T-A

18631645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480377-T-C

18631650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480382-A-G

http://identifiers.org/hco/20/GRCh38#18631670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144480409-C-A

18631670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480409-C-T

18631730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480469-T-C

18631734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480472-G-A

18631748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480486-T-C

18632190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480651-G-A

18632204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480665-T-C

18632240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480701-G-A

18632240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480701-G-C

18632241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 144480702-A-G

http://identifiers.org/hco/20/GRCh38#18632377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144480806-C-A

18632377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144480806-C-G

18632377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144480806-C-T

18632464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144480889-T-C

http://identifiers.org/hco/20/GRCh38#18632468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144480893-C-A

18632562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144480985-T-C

18632572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144480995-C-T

http://identifiers.org/hco/20/GRCh38#18632583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144481006-C-A

18632719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144481128-G-C

18632719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144481128-G-T

18634016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144482666-G-C

18634286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144482926-T-C

18634698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144483346-G-C

18634966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144483603-T-C

18634966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144483603-T-G

18635117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144483714-G-A

18635396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144483959-G-C

18635653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144484201-G-A

18635789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144484351-G-A

18635975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144484533-A-G

18636435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144484998-A-G

18636518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144485078-T-G

18636760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144485282-C-G

18636806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144485312-T-G

18637062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144485513-T-C

18637151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144485601-A-G

18637573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144485988-G-A

18637573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144485988-G-T

18637643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144486070-C-T

18637887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144486314-G-A

18638014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144486840-G-A

18638148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144486967-C-T

18638292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144487058-G-A

18638292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144487058-G-T

18638941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144487635-A-G

18638963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144487657-G-A

18639203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144487862-G-A

18639274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144487920-C-T

18639300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144487949-A-G

18639360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144488011-T-C

18639483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144488147-C-T

18639564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144488234-G-A

18639857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144488537-A-G

18640593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144489269-G-A

18640593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144489269-G-T

18640620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144489295-A-G

18640620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144489295-A-T

http://identifiers.org/hco/20/GRCh38#18643652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144490058-C-A

18643652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144490058-C-T

18644034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144490406-A-G

18644152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144490522-G-T

18644265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144490629-C-T

18644726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144491078-C-T

18645451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144491391-T-C

18645451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144491391-T-G

18645531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144491493-G-T

18646578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144492675-T-C

18646649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144492741-C-T

18646886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144492973-G-C

18646935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144493022-G-A

http://identifiers.org/hco/20/GRCh38#18646954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144493041-C-A

18646954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144493041-C-G

18647004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144493091-A-G

http://identifiers.org/hco/20/GRCh38#18647233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144493334-C-A

18647326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144493419-G-C

18647326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144493419-G-T

18647342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144493436-G-A

18649753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144495923-A-G

18649940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144496104-C-G

18650016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144496166-T-G

18650407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144496591-C-T

18650620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144496766-C-T

18650710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144496842-T-C

18651612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144497661-G-A

18651626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144497676-G-T

http://identifiers.org/hco/20/GRCh38#18651994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144497940-C-A

18652212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144498091-T-G

18652400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144498264-A-G

18652959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144501891-A-T

http://identifiers.org/hco/20/GRCh38#18653080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144502007-C-A

18653775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144502407-A-G

18653803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144502443-G-T

18653964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144502588-A-G

18656423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144505844-A-G

18656538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144505962-A-T

18656610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144506026-G-A

18656610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144506026-G-T

18656847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144506217-T-C

18656946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144506314-C-T

18657346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144506894-A-G

18657406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144506962-G-T

18657808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144507447-T-G

http://identifiers.org/hco/20/GRCh38#18657957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144507600-A-C

18660784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144508974-T-C

18664760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144513366-G-C

18664810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144513394-G-C

18664909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144513485-T-C

18665660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144514490-A-G

18666919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144518561-C-T

18666947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144518589-G-C

18666961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144518605-C-T

18666997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144518640-G-A

18667145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144518791-G-A

18667170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144518816-G-A

18667399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144519025-C-T

18667892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144519435-C-T

18667962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144519505-G-A

18668250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144519791-C-T

18668480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520021-G-A

18668480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520021-G-T

18668767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520256-T-C

http://identifiers.org/hco/20/GRCh38#18668795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144520288-C-A

18668795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520288-C-T

18668972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520463-G-A

18669101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520564-G-C

18669207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520688-G-A

18669411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520874-G-A

18669411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520874-G-T

18669442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520904-G-A

18669442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144520904-G-C

18669732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144521172-A-G

18669733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144521173-C-T

18669896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144521330-T-G

18670494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144521649-T-G

18670586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144521687-G-T

18670712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144521810-C-T

18670910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144521996-G-T

18670998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144522071-A-G

18671033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144522107-A-G

18671046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144522120-G-A

18671046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144522120-G-T

18671101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144522176-C-T

18671127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144522212-T-G

18671184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144522263-A-G

18671274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144522353-A-T

18671802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144523030-G-A

18672000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144523273-G-A

18672499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144523935-T-A

18672545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144523975-C-G

18672714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144524141-G-C

18673194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144524568-G-T

18673248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144524682-A-G

18673682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144525110-C-T

http://identifiers.org/hco/20/GRCh38#18673927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144525487-C-A

18674009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144525614-A-G

18674516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526126-G-T

18674521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526131-G-A

18674560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526167-A-G

18674714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526274-G-A

18674762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526319-G-A

18674762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526319-G-T

http://identifiers.org/hco/20/GRCh38#18674774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144526327-C-A

18674774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526327-C-T

http://identifiers.org/hco/20/GRCh38#18674938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144526441-C-A

18674938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526441-C-T

18675042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526542-A-T

18675114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526619-C-T

18675270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144526774-G-C

18677619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144537079-T-A

18677908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144537377-G-C

18678268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144537668-G-A

18678706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538022-T-C

18678750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538051-G-A

18678750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538051-G-C

18678750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538051-G-T

http://identifiers.org/hco/20/GRCh38#18678753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144538054-C-A

18678753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538054-C-T

18678754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538055-T-C

http://identifiers.org/hco/20/GRCh38#18678756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144538057-C-A

18678756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538057-C-T

18678885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538149-G-A

18678885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144538149-G-T

http://identifiers.org/hco/20/GRCh38#18678888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144538152-C-A

http://identifiers.org/hco/20/GRCh38#18678916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144538180-C-A

18687066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144539766-G-A

18687191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144539865-G-A

18687191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144539865-G-C

18687718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144540313-A-G

18688152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144540599-C-T

18688508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144540883-G-T

18688694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144541084-T-A

18688695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144541085-G-C

18688848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144541223-A-G

18688884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144541270-T-G

http://identifiers.org/hco/20/GRCh38#18688944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144541332-C-A

18689076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144541464-G-A

18689085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144541473-G-A

18689117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144541505-C-T

18689201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144541588-C-G

18692253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144542483-G-A

18692286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144542647-T-C

18692287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144542648-G-C

18692363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144542724-T-A

18692467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144542820-C-T

http://identifiers.org/hco/20/GRCh38#18693816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144544373-C-A

18694260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545051-G-A

18694265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545056-C-T

18694379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545152-C-T

18694533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545340-C-T

18694613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545416-A-G

http://identifiers.org/hco/20/GRCh38#18696221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144545662-C-A

18696504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545933-G-T

18696851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545963-G-C

18696851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545963-G-T

18696876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545995-C-G

http://identifiers.org/hco/20/GRCh38#18696877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#144545996-C-A

18696877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144545996-C-T

18698090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144546493-T-G

18701924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144547597-A-G

18701970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144547627-C-T

18702163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144547787-G-C

18702269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144547887-C-T

18702272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144547890-C-T

18707460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144548005-T-C

18707460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144548005-T-G

http://identifiers.org/hco/20/GRCh38#18707531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144548063-A-C

18707531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144548063-A-G

18707692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144548144-T-G

18709702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144551345-T-A

18709847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144551478-G-A

http://identifiers.org/hco/20/GRCh38#18710593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144554582-A-C

18710732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144554721-G-T

18710923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144554901-G-A

18712935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144560574-A-T

18713269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144560253-T-C

18713383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144560141-G-A

18714845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561023-C-G

18714846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561024-C-T

18714866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561044-A-G

18714993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561110-C-T

18715244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561298-C-T

18715278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561336-G-C

18715358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561410-G-C

18715400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561451-C-T

18715503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561512-A-G

18715814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561780-C-T

18715828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561794-G-A

18715909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561872-G-T

18715932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561893-G-A

18715982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561943-G-A

18716026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144561974-C-T

http://identifiers.org/hco/20/GRCh38#18716136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144562083-C-A

18716266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144562219-T-C

18721408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144565267-C-T

18721579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144565404-G-T

18721875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144565662-G-T

18721928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144565707-G-A

18721986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144565766-G-T

18722109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144565881-C-T

18722149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144565921-C-T

http://identifiers.org/hco/20/GRCh38#18722278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144565988-C-A

18722278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144565988-C-T

18722408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144566114-C-T

18722530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144566232-G-T

18722694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144566398-T-C

18722968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144566592-C-T

18722982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144566607-C-G

18723044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144566658-T-C

18723182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144566792-A-G

18723515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144567056-G-A

18723710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144567254-C-T

18723792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144567338-G-A

18724393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144569656-T-C

http://identifiers.org/hco/20/GRCh38#18724451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144569693-C-A

18724470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144569712-A-G

18724509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144569757-T-G

18724696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144569954-A-G

18725821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144570339-C-T

http://identifiers.org/hco/20/GRCh38#18726796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144571162-C-A

18727023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144571355-C-T

18727125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144571451-C-G

18727125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144571451-C-T

18727229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144571557-G-A

18727229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144571557-G-T

18727485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144571756-C-T

18727797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144572092-G-C

18728347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144573704-C-T

18729195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144574310-G-A

18729195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144574310-G-T

18729356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144574490-G-A

18729828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144574907-C-T

http://identifiers.org/hco/20/GRCh38#18729957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144575035-A-C

18730026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144575127-T-C

18730061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144575160-T-C

18730428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144575675-T-G

18730459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144575705-G-A

18730507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144575751-G-A

http://identifiers.org/hco/20/GRCh38#18730992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144578452-C-A

18731016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144578470-T-C

18731307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144578714-G-C

18731476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144578876-T-G

18731861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144579177-T-C

18732116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144579436-C-T

18732156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144579476-G-A

18732156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144579476-G-C

18732156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144579476-G-T

18732339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144579643-T-G

http://identifiers.org/hco/20/GRCh38#18732816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144580097-C-A

18733213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144580431-C-T

http://identifiers.org/hco/20/GRCh38#18733364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144580531-A-C

18733543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144580677-C-T

18733922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581027-G-A

18733922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581027-G-C

18733988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581090-T-A

18734244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581336-C-T

18734356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581450-G-A

18734358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581452-A-G

18734447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581829-C-G

18734481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581863-G-A

18734548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144581989-C-T

18734786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144582225-G-C

18734802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144582241-A-T

18734929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144582346-C-T

http://identifiers.org/hco/20/GRCh38#18735428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144582825-C-A

18736202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144583411-G-C

18736321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144583530-T-A

18736585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144583679-G-A

18736585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144583679-G-T

18736837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144583900-T-C

18737011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144584056-C-T

18737018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144584065-G-T

18737055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144584104-C-T

18739471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144584694-G-T

18739674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144584978-C-T

18739724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144585029-T-A

18740156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144585567-T-A

18740156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144585567-T-G

18740157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144585568-A-G

18740157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144585568-A-T

18741033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144586409-T-C

18741516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144587006-T-C

18742240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144587631-C-T

18743065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144588070-C-G

18743065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144588070-C-T

18743242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144588255-C-G

18743296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144588326-C-G

18744033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144588747-G-A

18744100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 144588821-C-G

18744100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 144588821-C-T

18744333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144589057-G-C

18744333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144589057-G-T

18745268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144589668-C-T

18745470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144589848-G-A

18750026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144594619-T-C

http://identifiers.org/hco/20/GRCh38#18750072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144594671-C-A

18750072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144594671-C-T

18750415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144594964-A-G

18750415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144594964-A-T

18750478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144595024-G-A

18750618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144595165-C-T

http://identifiers.org/hco/20/GRCh38#18750949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144595461-C-A

18754296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 144602487-G-A

18754689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144602583-G-A

18754689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144602583-G-T

http://identifiers.org/hco/20/GRCh38#18755023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144602900-C-A

18761980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144605828-G-A

18761982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144605830-G-C

18761989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144605837-T-G

18761993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144605838-C-T

18762145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144605996-T-C

18762284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144606092-C-T

18762336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144606119-A-G

18763173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144609946-G-A

http://identifiers.org/hco/20/GRCh38#18763268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144610047-C-A

18763268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 144610047-C-T

18763563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144610332-T-C

18763756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144610511-T-C

18763798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144610550-G-T

18763973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144610713-T-A

18764161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144610879-T-C

http://identifiers.org/hco/20/GRCh38#18764310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144610973-C-A

18764310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144610973-C-T

18764737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144611412-T-C

18765010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144611661-T-A

18765010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144611661-T-C

http://identifiers.org/hco/20/GRCh38#18765113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144611760-C-A

18765113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144611760-C-T

18765162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144611812-C-G

http://identifiers.org/hco/20/GRCh38#18765169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144611819-C-A

18765169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144611819-C-T

http://identifiers.org/hco/20/GRCh38#18765519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144612155-C-A

18765529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144612165-G-T

18765623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144612254-A-G

18765623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144612254-A-T

http://identifiers.org/hco/20/GRCh38#18765683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144612314-C-A

http://identifiers.org/hco/20/GRCh38#18765805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144612441-C-A

18765805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144612441-C-G

18765967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144612604-C-G

18765967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144612604-C-T

http://identifiers.org/hco/20/GRCh38#18766122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144612768-C-A

18766323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 144612971-G-A

http://identifiers.org/hco/20/GRCh38#18766405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16219
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#144613048-C-A